A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402487



Internal ID22460357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98040230..98041816hg38UCSC Ensembl
chr1:98505786..98507372hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381587
hg191587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878036
Supporting Variants
Samples
Known GenesMIR137HG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402487
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