A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131681



Internal ID18918905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:10416996..10417080hg38UCSC Ensembl
Outerchr3:10458680..10458764hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986173
SamplesKWS1
Known GenesATP2B2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131681
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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