A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571604



Internal ID20944675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131362943..131363673hg38UCSC Ensembl
chr5:130698636..130699366hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267912
Samples
Known GenesCDC42SE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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