A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347646



Internal ID21005199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241912101..242093600hg38UCSC Ensembl
chr2:242854252..243035751hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38181500
hg19181500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4330n223
Supporting Variantsnssv18084870
Samples
Known GenesLOC728323
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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