A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356698



Internal ID22582367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173525172..173526297hg38UCSC Ensembl
chr1:173494311..173495436hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870178
Supporting Variants
Samples
Known GenesSLC9C2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356698
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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