A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908683



Internal ID6270610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61558229..61616959hg19UCSC Ensembl
Outerchr17:61548948..61630076hg19UCSC Ensembl
Innerchr17:58911961..58970691hg18UCSC Ensembl
Outerchr17:58902680..58983808hg18UCSC 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 Variantsnssv1549929
SamplesMS18276
Known GenesACE, DCAF7, KCNH6
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908683
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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