A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361122



Internal ID22586791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26186514..26187661hg38UCSC Ensembl
chr1:26513005..26514152hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871638
Supporting Variants
Samples
Known GenesCNKSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361122
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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