A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515659



Internal ID15443270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21799836..21938800hg38UCSC Ensembl
Innerchr1:22126329..22265293hg19UCSC Ensembl
Innerchr1:21998916..22137880hg18UCSC Ensembl
Innerchr1:21871635..22010599hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38138965
hg19138965
hg18138965
hg17138965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664272, nssv669540, nssv663807, nssv705759, nssv669785, nssv705427, nssv687314, nssv704109, nssv695098
Samples
Known GenesHSPG2, LDLRAD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515659
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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