A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011017



Internal ID21920360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1624589..1643490hg38UCSC Ensembl
chr6:1624824..1643724hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3818902
hg1918901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571692
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011017
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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