A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443682



Internal ID21101235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125317152..125317460hg38UCSC Ensembl
chr9:128079431..128079739hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176681
Samples
Known GenesGAPVD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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