A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984868



Internal ID18865594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:32412192..32412792hg38UCSC Ensembl
Outerchr21:33784500..33785100hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126606
Supporting Variants
SamplesKWS1
Known GenesEVA1C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984868
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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