A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341117



Internal ID20998670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217177147..217177748hg38UCSC Ensembl
chr2:218041870..218042471hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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