A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147345



Internal ID346526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30945183..30953536hg38UCSC Ensembl
chr10:31234112..31242465hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg388354
hg198354
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030476
Samples
Known GenesZNF438
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147345
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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