A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435913



Internal ID21093466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88678527..88685110hg38UCSC Ensembl
chr9:91293442..91300025hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386584
hg196584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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