A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340929



Internal ID20998482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23503524..23507924hg38UCSC Ensembl
chr2:23726394..23730794hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg384401
hg194401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087384
Samples
Known GenesKLHL29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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