A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513566



Internal ID20886912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15964958..16196723hg38UCSC Ensembl
chr17:15868272..16100037hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38231766
hg19231766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182713
Samples
Known GenesADORA2B, NCOR1, TTC19, ZSWIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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