A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326925



Internal ID20860062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151260897..151261786hg38UCSC Ensembl
chr1:151233373..151234262hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051318
Samples
Known GenesPSMD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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