A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150256



Internal ID21444814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143875316..143878740hg38UCSC Ensembl
chr6:144196453..144199877hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383425
hg193425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580407
Supporting Variants
SamplesHG00732
Known GenesZC2HC1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150256
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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