A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908682



Internal ID6270609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61527677..61573761hg19UCSC Ensembl
Outerchr17:61496471..61578048hg19UCSC Ensembl
Innerchr17:58881409..58927493hg18UCSC Ensembl
Outerchr17:58850203..58931780hg18UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1543733
SamplesMS16153
Known GenesACE, CYB561, TANC2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908682
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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