A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343720



Internal ID21001273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150533940..150553066hg38UCSC Ensembl
chr2:151390454..151409580hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3819127
hg1919127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078444
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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