A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316564



Internal ID20849644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59939730..59961043hg38UCSC Ensembl
chr1:60405402..60426715hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3821314
hg1921314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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