A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332619



Internal ID20865792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78835830..78879646hg38UCSC Ensembl
chr1:79301515..79345331hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3843817
hg1943817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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