A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871638



Internal ID22646576
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 StatusM
Merged Variants
Supporting Variantsnssv17361122
Samples
Known GenesCNKSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871638
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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