A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1404e199



Internal ID22759177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144546624..144556471hg38UCSC Ensembl
chrX:143628145..143637992hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg389848
hg199848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675170, esv2671813
SamplesNA19648, NA20508, NA19664, NA18592, HG00559, HG00187, HG01188, NA18603, HG00640, NA19777, HG00449, NA20517, NA20507, HG01070, HG00272, NA19762, NA19728, HG00173, NA19723, NA19771, NA19782, NA19681, NA19079, NA19720, NA19651, NA19789, HG00154, HG00282, HG00245, HG00428, NA19717, HG00344, NA19788, NA12718, NA18630, NA19654, HG00324, NA19774, NA19655, NA20581, NA19750, NA19761, NA19682, NA20828, NA19756, NA20542, NA19675, NA18541, NA19685, NA19729, HG00124, NA19652, NA20801, HG01190, NA19749, NA19747, HG00565, HG00366, NA19732, NA19773, HG01174, NA19679, NA19786, NA19783, NA19759, HG00111, NA19785, NA20582, NA19716, NA19770, NA19726, NA19780, NA19661, NA19755, NA19758, HG00171, HG00554, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1404e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss78
Observed Complex0
Frequencyn/a


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