A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665400



Internal ID15055366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130347120..130388248hg38UCSC Ensembl
Innerchr7:129986961..130028089hg19UCSC Ensembl
Innerchr7:129774197..129815325hg18UCSC Ensembl
Innerchr7:129580912..129622040hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3841129
hg1941129
hg1841129
hg1741129
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515945
Supporting Variants
Samples
Known GenesCPA1, CPA5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665400
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