A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441567



Internal ID21099120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98598101..98599700hg38UCSC Ensembl
chr10:100357858..100359457hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985803
Samples
Known GenesHPSE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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