A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358578



Internal ID21016131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112141213..112145230hg38UCSC Ensembl
chr3:111860060..111864077hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg384018
hg194018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092119
Samples
Known GenesSLC9C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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