A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982191



Internal ID18871944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:156777666..156779566hg38UCSC Ensembl
Outerchr6:157098800..157100700hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145109
Supporting Variants
SamplesKWS1
Known GenesARID1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982191
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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