A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150005



Internal ID15508040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81406747..81526679hg38UCSC Ensembl
Innerchr17:79380547..79493705hg19UCSC Ensembl
Innerchr17:76995142..77108300hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38119933
hg19113159
hg18113159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576176
Supporting Variants
Samples1780862304_A
Known GenesACTG1, BAHCC1, MIR3186
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150005
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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