A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523181



Internal ID15103788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:156580462..156706761hg38UCSC Ensembl
Innerchr1:156550254..156676553hg19UCSC Ensembl
Innerchr1:154816878..154943177hg18UCSC Ensembl
Innerchr1:153363327..153489626hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38126300
hg19126300
hg18126300
hg17126300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698894
Samples
Known GenesAPOA1BP, BCAN, CRABP2, GPATCH4, HAPLN2, NES, TTC24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523181
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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