A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478958



Internal ID21136511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79542028..79542669hg38UCSC Ensembl
chr13:80116163..80116804hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013481
Samples
Known GenesNDFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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