A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866769



Internal ID15814039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10762033..10814772hg38UCSC Ensembl
Innerchr17:10665350..10718089hg19UCSC Ensembl
Innerchr17:10606075..10658814hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3852740
hg1952740
hg1852740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574351
Supporting Variants
Samples
Known GenesLINC00675, TMEM220-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866769
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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