A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347362



Internal ID21004915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62570299..62571729hg38UCSC Ensembl
chr2:62797434..62798864hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381431
hg191431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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