A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440436



Internal ID21097989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77028222..77028801hg38UCSC Ensembl
chr10:78787980..78788559hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984311
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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