A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451889



Internal ID21109442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23862941..23877178hg38UCSC Ensembl
chr10:24151870..24166107hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3814238
hg1914238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979759
Samples
Known GenesKIAA1217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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