A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672644



Internal ID15062610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130362476..130386054hg38UCSC Ensembl
Innerchr7:130002317..130025895hg19UCSC Ensembl
Innerchr7:129789553..129813131hg18UCSC Ensembl
Innerchr7:129596268..129619846hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3823579
hg1923579
hg1823579
hg1723579
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)nssv672644
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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