A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515666



Internal ID15096273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158255035..158267272hg38UCSC Ensembl
Innerchr1:158224825..158237062hg19UCSC Ensembl
Innerchr1:156491449..156503686hg18UCSC Ensembl
Innerchr1:155037898..155050135hg17UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3812238
hg1912238
hg1812238
hg1712238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664298, nssv660921, nssv659323, nssv665215
Samples
Known GenesCD1A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515666
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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