A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973716



Internal ID19246078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37384619..37384686hg38UCSC Ensembl
Outerchr20:36013022..36013089hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138957
Supporting Variants
SamplesKWS2
Known GenesSRC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973716
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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