A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964105



Internal ID18897801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:159934710..159934815hg38UCSC Ensembl
Outerchr6:160355742..160355847hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120897
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964105
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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