A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956785



Internal ID17305658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:39216991..39217081hg38UCSC Ensembl
Outerchr21:40588917..40589007hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003344
SamplesBILGI_BIOE
Known GenesBRWD1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956785
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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