A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845210



Internal ID22620145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2947426..2949025hg38UCSC Ensembl
chr6:2947660..2949259hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504444
Samples
Known GenesSERPINB6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845210
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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