A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126657



Internal ID18940321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:141876358..141877258hg38UCSC Ensembl
Outerchr3:141595200..141596100hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984923
SamplesKWS1
Known GenesATP1B3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126657
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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