A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704497



Internal ID15441149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38278989..38303396hg38UCSC Ensembl
Innerchr7:38318590..38342997hg19UCSC Ensembl
Innerchr7:38285115..38309522hg18UCSC Ensembl
Innerchr7:38091830..38116237hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3824408
hg1924408
hg1824408
hg1724408
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)nssv704497
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