A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986082



Internal ID19224340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:13957690..13957760hg38UCSC Ensembl
Outerchr21:15330011..15330081hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131620
Supporting Variants
SamplesKWS1
Known GenesANKRD20A11P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986082
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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