A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576177



Internal ID16016900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81450374..81483574hg38UCSC Ensembl
Innerchr17:79417400..79450600hg19UCSC Ensembl
Innerchr17:77031995..77065195hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3833201
hg1933201
hg1833201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877112
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576177
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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