A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417100



Internal ID21074653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18517777..18654640hg38UCSC Ensembl
chr9:18517775..18654638hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38136864
hg19136864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175485
Samples
Known GenesADAMTSL1, MIR3152
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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