A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347681



Internal ID21005234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219101101..219103900hg38UCSC Ensembl
chr2:219965823..219968622hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085498
Samples
Known GenesNHEJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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