A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798028



Internal ID21243366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63501226..63501365hg38UCSC Ensembl
chr17:61578587..61578726hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798028
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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