A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348829



Internal ID21006382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:185438501..185678100hg38UCSC Ensembl
chr2:186303228..186542827hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38239600
hg19239600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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