A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv865020



Internal ID15812290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:632287..745992hg38UCSC Ensembl
Innerchr17:535527..649232hg19UCSC Ensembl
Innerchr17:482277..595982hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38113706
hg19113706
hg18113706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574075
Supporting Variants
Samples
Known GenesFAM57A, GEMIN4, VPS53
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv865020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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