A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832187



Internal ID22607122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211481512..211524456hg38UCSC Ensembl
chr2:212346237..212389181hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3842945
hg1942945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482074, nssv17482075
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832187
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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