A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832807



Internal ID22607742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231507046..231508263hg38UCSC Ensembl
chr2:232371757..232372974hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381218
hg191218
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832807
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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