A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322519



Internal ID20855632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13513001..13515200hg38UCSC Ensembl
chr1:13839496..13841695hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200109
Samples
Known GenesLRRC38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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