A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442000



Internal ID21099553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24315642..24318050hg38UCSC Ensembl
chr10:24604571..24606979hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382409
hg192409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979250
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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