A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972239



Internal ID19205902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111882647..111882965hg38UCSC Ensembl
Outerchr6:112203850..112204168hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123238
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972239
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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