A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995945



Internal ID18845122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:38491959..38492071hg38UCSC Ensembl
Outerchr21:39863883..39863995hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146789
Supporting Variants
SamplesKWB1
Known GenesERG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3995945
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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