A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324083



Internal ID20857207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99119259..99119704hg38UCSC Ensembl
chr1:99584815..99585260hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065983
Samples
Known GenesLOC100129620
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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