A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319565



Internal ID20852660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151749244..151758083hg38UCSC Ensembl
chr1:151721720..151730559hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg388840
hg198840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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