A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434041



Internal ID21091594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5654360..5655940hg38UCSC Ensembl
chr9:5654360..5655940hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381581
hg191581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188169
Samples
Known GenesKIAA1432
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434041
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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