A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350325



Internal ID21007878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13343501..13345200hg38UCSC Ensembl
chr2:13483626..13485325hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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