A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833702



Internal ID22608637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69789579..69794763hg38UCSC Ensembl
chr2:70016711..70021895hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg385185
hg195185
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487993
Samples
Known GenesANXA4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833702
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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