A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350211



Internal ID21007764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216544751..216546550hg38UCSC Ensembl
chr2:217409474..217411273hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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