A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576098



Internal ID16016821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78564295..78599049hg38UCSC Ensembl
Innerchr17:76560377..76595131hg19UCSC Ensembl
Innerchr17:74071972..74106726hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3834755
hg1934755
hg1834755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149438
Samples1780862586_A
Known GenesDNAH17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576098
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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