A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670708



Internal ID15407360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17737040..17754252hg38UCSC Ensembl
Innerchr11:17758587..17775799hg19UCSC Ensembl
Innerchr11:17715163..17732375hg18UCSC Ensembl
Innerchr11:17715163..17732375hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3817213
hg1917213
hg1817213
hg1717213
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516767
Supporting Variants
Samples
Known GenesKCNC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670708
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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