A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150004



Internal ID15876275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81216762..81282974hg38UCSC Ensembl
Innerchr17:79190562..79256774hg19UCSC Ensembl
Innerchr17:76805157..76871369hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3866213
hg1966213
hg1866213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576172
Supporting Variants
SamplesHGDP00814
Known GenesAZI1, C17orf89, ENTHD2, SLC38A10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150004
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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