A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877117



Internal ID16171073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81537989..81551343hg38UCSC Ensembl
Innerchr17:79505015..79518369hg19UCSC Ensembl
Innerchr17:77115491..77128811hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3813355
hg1913355
hg1813321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576182
Supporting Variants
Samples
Known GenesC17orf70
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877117
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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