A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627074



Internal ID21575379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37936021..37936021hg38UCSC Ensembl
chr7:37975623..37975623hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151006
SamplesHG03065
Known GenesEPDR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627074
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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