A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv877112



Internal ID15824382
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 StatusS
Merged Variantsnsv576177
Supporting Variants
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv877112
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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