A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370312



Internal ID21027865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126951544..127017507hg38UCSC Ensembl
chr3:126670387..126736350hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3865964
hg1965964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094083
Samples
Known GenesCHCHD6, PLXNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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