A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336203



Internal ID20993756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154792801..154795800hg38UCSC Ensembl
chr2:155649313..155652312hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080125
Samples
Known GenesKCNJ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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