A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347712



Internal ID21005265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186976424..187058682hg38UCSC Ensembl
chr2:187841151..187923409hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3882259
hg1982259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347712
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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