A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150514



Internal ID21503289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49133125..49140425hg38UCSC Ensembl
chr7:49172721..49180021hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg387301
hg197301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568634
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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