A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440543



Internal ID21098096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17657212..17659418hg38UCSC Ensembl
chr10:17699211..17701417hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg382207
hg192207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978993
Samples
Known GenesSTAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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