A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332847



Internal ID20866022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23722210..23731861hg38UCSC Ensembl
chr1:24048700..24058351hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg389652
hg199652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv121n223
Supporting Variantsnssv18058970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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