A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533313



Internal ID20906674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82294456..82671315hg38UCSC Ensembl
chr17:80252332..80629191hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38376860
hg19376860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3259n223
Supporting Variantsnssv18186033
Samples
Known GenesC17orf62, CD7, FOXK2, HEXDC, NARF, OGFOD3, RAB40B, SECTM1, TEX19, UTS2R, WDR45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533313
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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