A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973740



Internal ID19234031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62971505..62971562hg38UCSC Ensembl
Outerchr20:61602857..61602914hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136563
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973740
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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