A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652854



Internal ID15042820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21537198..21662129hg38UCSC Ensembl
Innerchr1:21863691..21988622hg19UCSC Ensembl
Innerchr1:21736278..21861209hg18UCSC Ensembl
Innerchr1:21608997..21733928hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38124932
hg19124932
hg18124932
hg17124932
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517096
Supporting Variants
Samples
Known GenesALPL, RAP1GAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652854
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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