A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150008



Internal ID15530196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82035336..82176517hg38UCSC Ensembl
Innerchr17:79993212..80134393hg19UCSC Ensembl
Innerchr17:77586501..77727682hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38141182
hg19141182
hg18141182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576187
Supporting Variants
SamplesHGDP00908
Known GenesCCDC57, DCXR, DUS1L, FASN, GPS1, RFNG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150008
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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