A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832636



Internal ID22607571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37085674..37087073hg38UCSC Ensembl
chr2:37312817..37314216hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484792, nssv17484793
Samples
Known GenesGPATCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832636
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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