A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701002



Internal ID15437654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38278989..38317722hg38UCSC Ensembl
Innerchr7:38318590..38357323hg19UCSC Ensembl
Innerchr7:38285115..38323848hg18UCSC Ensembl
Innerchr7:38091830..38130563hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3838734
hg1938734
hg1838734
hg1738734
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519863
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701002
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