A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702360



Internal ID15439012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75364822..75369876hg38UCSC Ensembl
Innerchr11:75075866..75080920hg19UCSC Ensembl
Innerchr11:74753514..74758568hg18UCSC Ensembl
Innerchr11:74753514..74758568hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385055
hg195055
hg185055
hg175055
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv702360
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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