A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899990



Internal ID22675127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149480791..149481749hg38UCSC Ensembl
chr6:149801927..149802885hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38959
hg19959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410580
Samples
Known GenesZC3H12D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899990
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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