A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704745



Internal ID15441397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62892897..62977911hg38UCSC Ensembl
Innerchr7:62353275..62438289hg19UCSC Ensembl
Innerchr7:61990710..62075724hg18UCSC Ensembl
Innerchr7:61797425..61882439hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3885015
hg1985015
hg1885015
hg1785015
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704745
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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