A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315721



Internal ID20848793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30086205..30706381hg38UCSC Ensembl
chr1:30559052..31179228hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38620177
hg19620177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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