A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435599



Internal ID21093152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32351859..32356432hg38UCSC Ensembl
chr10:32640787..32645360hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg384574
hg194574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980055
Samples
Known GenesEPC1, LOC102031319
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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