A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349243



Internal ID21006796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23484027..23491203hg38UCSC Ensembl
chr2:23706897..23714073hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg387177
hg197177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087373
Samples
Known GenesKLHL29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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