A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689106



Internal ID15425758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43375407..43384513hg38UCSC Ensembl
Innerchr7:43415006..43424112hg19UCSC Ensembl
Innerchr7:43381531..43390637hg18UCSC Ensembl
Innerchr7:43188246..43197352hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg389107
hg199107
hg189107
hg179107
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521089
Supporting Variants
Samples
Known GenesHECW1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689106
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