A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077251



Internal ID19320784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153201986..153230587hg38UCSC Ensembl
chrX:152434799..152463400hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3828602
hg1928602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767309
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077251
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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