A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354036



Internal ID21011589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24034290..24035649hg38UCSC Ensembl
chr2:24257160..24258519hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381360
hg191360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084539
Samples
Known GenesC2orf44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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