A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443811



Internal ID21101364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74131426..74131801hg38UCSC Ensembl
chr10:75891184..75891559hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983892
Samples
Known GenesAP3M1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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