A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584608



Internal ID20957679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30982854..31221335hg38UCSC Ensembl
chr14:31452060..31690541hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38238482
hg19238482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227725
Samples
Known GenesAP4S1, HECTD1, MIR624, STRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584608
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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