A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449994



Internal ID21107547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31948260..31952117hg38UCSC Ensembl
chr10:32237188..32241045hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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