A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519667



Internal ID15446960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140269251..140292587hg38UCSC Ensembl
Innerchr7:139969051..139992387hg19UCSC Ensembl
Innerchr7:139615520..139638856hg18UCSC Ensembl
Innerchr7:139422235..139445571hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3823337
hg1923337
hg1823337
hg1723337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696982
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519667
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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