A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576175



Internal ID16016898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81349843..81509075hg38UCSC Ensembl
Innerchr17:79323643..79476101hg19UCSC Ensembl
Innerchr17:76938238..77090696hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38159233
hg19152459
hg18152459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877111
Samples
Known GenesBAHCC1, LOC100130370, MIR3186, MIR4740
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576175
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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