A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330681



Internal ID20863839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183613401..183619000hg38UCSC Ensembl
chr1:183582536..183588135hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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