A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322110



Internal ID20855220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98036672..98037235hg38UCSC Ensembl
chr1:98502228..98502791hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065788
Samples
Known GenesMIR137HG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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