A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443031



Internal ID21100584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36894976..36897650hg38UCSC Ensembl
chr10:37183904..37186578hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg382675
hg192675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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