A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143112



Internal ID21507028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157441650..157441878hg38UCSC Ensembl
chr7:157234344..157234572hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576158
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143112
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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