A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347330



Internal ID21004883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215316987..215342814hg38UCSC Ensembl
chr2:216181710..216207537hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3825828
hg1925828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084029
Samples
Known GenesATIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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