A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576073



Internal ID16016796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77059838..77101828hg38UCSC Ensembl
Innerchr17:75055920..75097910hg19UCSC Ensembl
Innerchr17:72567515..72609505hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3841991
hg1941991
hg1841991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5784n54
Supporting Variantsnssv876224
Samples
Known GenesLINC00338, MIR6516, SCARNA16, SEC14L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576073
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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