A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440224



Internal ID21097777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36624990..36626680hg38UCSC Ensembl
chr10:36913918..36915608hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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