A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966845



Internal ID18897497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:104774076..104774389hg38UCSC Ensembl
Outerchr6:105221951..105222264hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130535
Supporting Variants
SamplesKWS2
Known GenesHACE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966845
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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