A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574607



Internal ID21523024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97970369..97970682hg38UCSC Ensembl
chr7:97599681..97599994hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155463
SamplesHG03371
Known GenesMGC72080
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574607
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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