A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432857



Internal ID21090410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16657131..16683846hg38UCSC Ensembl
chr9:16657129..16683844hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3826716
hg1926716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175750
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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