A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328407



Internal ID20861555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51671331..51671968hg38UCSC Ensembl
chr1:52137003..52137640hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062006
Samples
Known GenesOSBPL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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