A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862092



Internal ID22637027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131254430..131264640hg38UCSC Ensembl
chr7:130939189..130949399hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3810211
hg1910211
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501262
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862092
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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