A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447263



Internal ID21104816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76898201..76899300hg38UCSC Ensembl
chr10:78657959..78659058hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983479
Samples
Known GenesKCNMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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