A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339409



Internal ID20996962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162753001..162772300hg38UCSC Ensembl
chr2:163609511..163628810hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3819300
hg1919300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080239
Samples
Known GenesKCNH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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