A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432782



Internal ID21090335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29241044..29253647hg38UCSC Ensembl
chr9:29241042..29253645hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3812604
hg1912604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432782
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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