A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576986



Internal ID21525432
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 Variantsnssv17151479
SamplesHG02818
Known GenesZC3H12D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576986
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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