A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430971



Internal ID21088524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16592901..16594200hg38UCSC Ensembl
chr9:16592899..16594198hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175745
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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