A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509509



Internal ID20882819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29643399..29644978hg38UCSC Ensembl
chr17:27970417..27971996hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188569
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509509
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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