A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430983



Internal ID21088536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101852382..101884632hg38UCSC Ensembl
chr8:102864610..102896860hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3832251
hg1932251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161422
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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