A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389432



Internal ID21046985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:22131677..22558617hg38UCSC Ensembl
chr5:22131786..22558726hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38426941
hg19426941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128837
Samples
Known GenesCDH12, PMCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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