A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320864



Internal ID20853965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104015884..104193247hg38UCSC Ensembl
chr1:104558506..104735869hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38177364
hg19177364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051019
Samples
Known GenesLOC100129138
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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