A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317766



Internal ID20850855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56065229..56065818hg38UCSC Ensembl
chr1:56530902..56531491hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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