A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958543



Internal ID18860382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:106558161..106558231hg38UCSC Ensembl
Outerchr6:107006036..107006106hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128268
Supporting Variants
SamplesKWS1
Known GenesAIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958543
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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