A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327119



Internal ID20860256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119369477..119371013hg38UCSC Ensembl
chr1:119912100..119913636hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051259
Samples
Known GenesHAO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327119
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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