A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339094



Internal ID20996647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241270872..241271673hg38UCSC Ensembl
chr2:242210287..242211088hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085143
Samples
Known GenesHDLBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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