A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876257



Internal ID22651217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159968040..159975066hg38UCSC Ensembl
chr1:159937830..159944856hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg387027
hg197027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362285
Samples
Known GenesLINC01133
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876257
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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