A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370814



Internal ID22596483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6638184..6638240hg38UCSC Ensembl
chr17:6541504..6541560hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945842
Supporting Variants
Samples
Known GenesKIAA0753
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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