A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077247



Internal ID18979081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150983426..150984627hg38UCSC Ensembl
chrX:150151899..150153100hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766081
SamplesKWP1
Known GenesHMGB3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077247
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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