A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526682



Internal ID20900043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78506201..78513500hg38UCSC Ensembl
chr17:76502283..76509582hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038106
Samples
Known GenesDNAH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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