A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334498



Internal ID20867684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78694381..78694456hg38UCSC Ensembl
chr1:79160066..79160141hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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