A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336365



Internal ID20993918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175942347..175942986hg38UCSC Ensembl
chr2:176807075..176807714hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082024
Samples
Known GenesKIAA1715
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336365
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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