A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388332



Internal ID22446202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7874623..7881436hg38UCSC Ensembl
chr17:7777941..7784754hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386814
hg196814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388332
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