A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697631



Internal ID15434283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111438856..111559715hg38UCSC Ensembl
Innerchr7:111078912..111199771hg19UCSC Ensembl
Innerchr7:110866148..110987007hg18UCSC Ensembl
Innerchr7:110672863..110793722hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38120860
hg19120860
hg18120860
hg17120860
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697631
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