A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144019



Internal ID21450992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36515050..36515279hg38UCSC Ensembl
chr7:36554656..36554885hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566460
Supporting Variants
SamplesHG01505
Known GenesAOAH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144019
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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