A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087010



Internal ID21996243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88478812..88478812hg38UCSC Ensembl
chr9:91093727..91093727hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087010
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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