A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153600



Internal ID21424891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14379812..14379887hg38UCSC Ensembl
chr7:14419437..14419512hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574703
Supporting Variants
SamplesHG00731
Known GenesDGKB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153600
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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