A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436361



Internal ID21093914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130206834..130212298hg38UCSC Ensembl
chr9:132969113..132974577hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385465
hg195465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174678
Samples
Known GenesNCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436361
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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