A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346962



Internal ID21004515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175935263..175935893hg38UCSC Ensembl
chr2:176799991..176800621hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082022
Samples
Known GenesKIAA1715
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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