A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv651919



Internal ID15041885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2610039..2700381hg38UCSC Ensembl
Innerchr7:2649673..2740015hg19UCSC Ensembl
Innerchr7:2616199..2706541hg18UCSC Ensembl
Innerchr7:2422914..2513256hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3890343
hg1990343
hg1890343
hg1790343
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517403
Supporting Variants
Samples
Known GenesAMZ1, IQCE, TTYH3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv651919
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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