A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975828



Internal ID18883151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:110830045..110830111hg38UCSC Ensembl
Outerchr6:111151248..111151314hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137137
Supporting Variants
SamplesKWS2
Known GenesAMD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975828
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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