A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149813



Internal ID15508795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77313269..77348945hg38UCSC Ensembl
Innerchr17:75309351..75345027hg19UCSC Ensembl
Innerchr17:72820946..72856622hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3835677
hg1935677
hg1835677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576091
Supporting Variants
Samples1782681080_A
Known GenesSEPT9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149813
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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