A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676837



Internal ID15066803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21562847..21563142hg38UCSC Ensembl
Innerchr1:21889340..21889635hg19UCSC Ensembl
Innerchr1:21761927..21762222hg18UCSC Ensembl
Innerchr1:21634646..21634941hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38296
hg19296
hg18296
hg17296
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517096
Supporting Variants
Samples
Known GenesALPL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676837
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer