A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699693



Internal ID15436345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:75543817..75547087hg38UCSC Ensembl
Innerchr7:75173135..75176385hg19UCSC Ensembl
Innerchr7:75011071..75014321hg18UCSC Ensembl
Innerchr7:74817786..74821036hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383271
hg193251
hg183251
hg173251
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523858
Supporting Variants
Samples
Known GenesHIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699693
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