A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637178



Internal ID21585483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79014067..79014067hg38UCSC Ensembl
chr6:79723784..79723784hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146496
SamplesNA19239
Known GenesPHIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637178
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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