A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503032



Internal ID20876282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1439822..1440278hg38UCSC Ensembl
chr17:1343116..1343572hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188800
Samples
Known GenesCRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer