A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653987



Internal ID15390639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7243084..7253416hg38UCSC Ensembl
Innerchr5:7243197..7253529hg19UCSC Ensembl
Innerchr5:7296197..7306529hg18UCSC Ensembl
Innerchr5:7296197..7306529hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3810333
hg1910333
hg1810333
hg1710333
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517195
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653987
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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