A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517954



Internal ID15445247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137196006..137198178hg38UCSC Ensembl
Innerchr7:136880753..136882925hg19UCSC Ensembl
Innerchr7:136531293..136533465hg18UCSC Ensembl
Innerchr7:136338008..136340180hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382173
hg192173
hg182173
hg172173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695365
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517954
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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