A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328995



Internal ID20862146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73797443..74189227hg38UCSC Ensembl
chr1:74263126..74654911hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38391785
hg19391786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204395
Samples
Known GenesLRRIQ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328995
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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