A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439740



Internal ID21097293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115667901..115672200hg38UCSC Ensembl
chr9:118430180..118434479hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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