A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320898



Internal ID20853999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118544710..118545044hg38UCSC Ensembl
chr1:119087333..119087667hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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