A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549885



Internal ID15990608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5100663..5133258hg38UCSC Ensembl
Innerchr10:5142855..5175450hg19UCSC Ensembl
Innerchr10:5132855..5165450hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3832596
hg1932596
hg1832596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174109
SamplesNINDS_235
Known GenesAKR1C3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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