A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443646



Internal ID21101199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101210910..101250028hg38UCSC Ensembl
chr9:103973192..104012310hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3839119
hg1939119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171616
Samples
Known GenesLPPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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