A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039627



Internal ID21948970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91965595..93940605hg38UCSC Ensembl
chr13:92617849..94592858hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381975011
hg191975010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603537
Samples
Known GenesGPC5, GPC5-AS1, GPC6, GPC6-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039627
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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