A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580048



Internal ID21528534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149017591..149017678hg38UCSC Ensembl
chr7:148714683..148714770hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157594
SamplesNA19983
Known GenesPDIA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580048
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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