A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153387



Internal ID21505708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129214931..129216102hg38UCSC Ensembl
chr7:128854772..128855943hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg381172
hg191172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569655
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153387
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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