A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831374



Internal ID22606309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156341120..156342748hg38UCSC Ensembl
chr2:157197632..157199260hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg381629
hg191629
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488213, nssv17488212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831374
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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