A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908226



Internal ID6270153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:38878827..38957953hg19UCSC Ensembl
Outerchr17:38876409..39003217hg19UCSC Ensembl
Innerchr17:36132353..36211479hg18UCSC Ensembl
Outerchr17:36129935..36256743hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1599444
SamplesIS41634
Known GenesKRT10, KRT25, KRT26, KRT27, KRT28, TMEM99
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908226
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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