A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346622



Internal ID21004175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160324889..160329643hg38UCSC Ensembl
chr2:161181400..161186154hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg384755
hg194755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080528
Samples
Known GenesRBMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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