A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698102



Internal ID15434754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75360739..75369025hg38UCSC Ensembl
Innerchr11:75071783..75080069hg19UCSC Ensembl
Innerchr11:74749431..74757717hg18UCSC Ensembl
Innerchr11:74749431..74757717hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg388287
hg198287
hg188287
hg178287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516556
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698102
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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