A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319488



Internal ID20852583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212854114..212855842hg38UCSC Ensembl
chr1:213027456..213029184hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381729
hg191729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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