A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435225



Internal ID21092778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15879699..15880183hg38UCSC Ensembl
chr9:15879697..15880181hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175694
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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