A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683155



Internal ID15073121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21556327..21632043hg38UCSC Ensembl
Innerchr1:21882820..21958536hg19UCSC Ensembl
Innerchr1:21755407..21831123hg18UCSC Ensembl
Innerchr1:21628126..21703842hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3875717
hg1975717
hg1875717
hg1775717
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)nssv683155
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