A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557988



Internal ID20931059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112261525..112263803hg38UCSC Ensembl
chr3:111980372..111982650hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg382279
hg192279
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259201
Samples
Known GenesSLC9C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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