A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183574



Internal ID20750614
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 StatusS
Merged Variantsnsv6518157
Supporting Variants
Samples
Known GenesLINC00469, LOC100134391, LOC400620, MGC16275, RPL38, SDK2, TTYH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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