A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140832



Internal ID18934255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:103338356..103338422hg38UCSC Ensembl
Outerchr7:102978803..102978869hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992336
SamplesKWS2
Known GenesDNAJC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140832
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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