A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843572



Internal ID22618507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88836261..88837660hg38UCSC Ensembl
chr5:88132078..88133477hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499526, nssv17499527
Samples
Known GenesMEF2C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843572
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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