A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436260



Internal ID21093813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97443675..97450041hg38UCSC Ensembl
chr10:99203432..99209798hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg386367
hg196367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985999
Samples
Known GenesEXOSC1, ZDHHC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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