A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984067



Internal ID19206063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:23734030..23809845hg38UCSC Ensembl
Outerchr20:23714667..23790482hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3875816
hg1975816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125860
Supporting Variants
SamplesKWS1
Known GenesCST1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984067
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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