A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441371



Internal ID21098924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128899286..128928193hg38UCSC Ensembl
chr9:131661565..131690472hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3828908
hg1928908
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235756
Samples
Known GenesLRRC8A, PHYHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441371
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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