A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973799



Internal ID18879238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:33166986..33167085hg38UCSC Ensembl
Outerchr21:34539292..34539391hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114286
Supporting Variants
SamplesKWS2
Known GenesC21orf54
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973799
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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