A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875646



Internal ID15822916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59131391..59266820hg38UCSC Ensembl
Innerchr17:57208752..57344181hg19UCSC Ensembl
Innerchr17:54563534..54698963hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38135430
hg19135430
hg18135430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575802
Supporting Variants
Samples
Known GenesGDPD1, MIR301A, MIR454, PRR11, SKA2, SMG8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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