A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520148



Internal ID15100755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16005414..16139508hg38UCSC Ensembl
Innerchr1:16331909..16466003hg19UCSC Ensembl
Innerchr1:16204496..16338590hg18UCSC Ensembl
Innerchr1:16077215..16211309hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38134095
hg19134095
hg18134095
hg17134095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697249
Samples
Known GenesC1orf64, CLCNKA, CLCNKB, EPHA2, FAM131C, HSPB7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520148
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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