A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980203



Internal ID19216090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:146810223..146817120hg38UCSC Ensembl
Outerchr6:147131359..147138256hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg386898
hg196898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118001
Supporting Variants
SamplesKWS1
Known GenesADGB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980203
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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