A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440685



Internal ID21098238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109618223..109622405hg38UCSC Ensembl
chr9:112380503..112384685hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg384183
hg194183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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