A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875713



Internal ID15822983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60451344..60488871hg38UCSC Ensembl
Innerchr17:58528705..58566232hg19UCSC Ensembl
Innerchr17:55883487..55921014hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3837528
hg1937528
hg1837528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575827
Supporting Variants
Samples
Known GenesAPPBP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875713
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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