A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000695



Internal ID16946961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44112820..44155617hg38UCSC Ensembl
Outerchr21:45532701..45575500hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3842798
hg1942800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953644
Supporting Variants
SamplesBILGI_BIOE
Known GenesC21orf33, PWP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000695
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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