A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347629



Internal ID21005182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165977201..165978723hg38UCSC Ensembl
chr2:166833711..166835233hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381523
hg191523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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