A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436144



Internal ID21093697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96847001..96897400hg38UCSC Ensembl
chr9:99609283..99659682hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3850400
hg1950400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218688
Samples
Known GenesLOC100132781, ZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436144
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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