A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441786



Internal ID21099339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29944081..30047172hg38UCSC Ensembl
chr10:30233010..30336101hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38103092
hg19103092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981381
Samples
Known GenesKIAA1462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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