A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347543



Internal ID21005096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149301261..149309257hg38UCSC Ensembl
chr2:150157775..150165771hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg387997
hg197997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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