A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660921



Internal ID15050887
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515666
Supporting Variants
Samples
Known GenesCD1A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660921
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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