A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072602



Internal ID21981835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90684162..90684162hg38UCSC Ensembl
chr8:91696390..91696390hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38822
hg19822
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072602
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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