A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325349



Internal ID20858480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160799701..160805200hg38UCSC Ensembl
chr1:160769491..160774990hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200987
Samples
Known GenesLY9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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