A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368965



Internal ID21026518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128973551..128979966hg38UCSC Ensembl
chr3:128692394..128698809hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg386416
hg196416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093206
Samples
Known GenesKIAA1257
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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