A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518157



Internal ID20891518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73533474..74269733hg38UCSC Ensembl
chr17:71529613..72265872hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38736260
hg19736260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183574
Samples
Known GenesLINC00469, LOC100134391, LOC400620, MGC16275, RPL38, SDK2, TTYH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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