A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436764



Internal ID21094317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119231376..119231881hg38UCSC Ensembl
chr9:121993654..121994159hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175428
Samples
Known GenesBRINP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436764
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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