A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483330



Internal ID22541237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231888517..231899486hg38UCSC Ensembl
chr2:232753227..232764196hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3810970
hg1910970
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832243
Supporting Variants
Samples
Known GenesMIR1471
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483330
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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