A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429996



Internal ID21087549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14876596..14976321hg38UCSC Ensembl
chr9:14876594..14976319hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3899726
hg1999726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175004
Samples
Known GenesFREM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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