A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444697



Internal ID21102250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23893901..24339100hg38UCSC Ensembl
chr10:24182830..24628029hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38445200
hg19445200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979015
Samples
Known GenesKIAA1217, MIR603
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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