A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531441



Internal ID20904802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74732546..74733636hg38UCSC Ensembl
chr17:72728685..72729775hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193743
Samples
Known GenesRAB37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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