A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988332



Internal ID19203647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:1673959..1682838hg38UCSC Ensembl
Outerchr6:1674193..1683072hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg388880
hg198880
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133369
Supporting Variants
SamplesKWS1
Known GenesGMDS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988332
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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