A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960724



Internal ID18873659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:666300..667900hg38UCSC Ensembl
Outerchr6:666300..667900hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111822
Supporting Variants
SamplesKWS1
Known GenesEXOC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960724
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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