A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441782



Internal ID21099335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116810692..116845773hg38UCSC Ensembl
chr9:119572971..119608052hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3835082
hg1935082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174177
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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