A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855377



Internal ID22630312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52647344..52650900hg38UCSC Ensembl
chr12:53041128..53044684hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg383557
hg193557
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457587
Samples
Known GenesKRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855377
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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