A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317142



Internal ID20850226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153155710..153159682hg38UCSC Ensembl
chr1:153128186..153132158hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383973
hg193973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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