A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339264



Internal ID20996817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160307844..160310866hg38UCSC Ensembl
chr2:161164355..161167377hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg383023
hg193023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080527
Samples
Known GenesRBMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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