A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074124



Internal ID21983357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97178828..97178828hg38UCSC Ensembl
chr7:96808140..96808140hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562358
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074124
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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