A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332963



Internal ID20866138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234002101..234005000hg38UCSC Ensembl
chr1:234137847..234140746hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059034
Samples
Known GenesSLC35F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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