A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000666



Internal ID17293618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:31555388..31560387hg38UCSC Ensembl
Outerchr21:32927701..32932700hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953353
Supporting Variants
SamplesBILGI_BIOE
Known GenesTIAM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000666
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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