A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317727



Internal ID20850815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234692101..234835000hg38UCSC Ensembl
chr1:234827848..234970747hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38142900
hg19142900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv556n223
Supporting Variantsnssv18202395
Samples
Known GenesLINC01132
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317727
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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