A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581590



Internal ID20954661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67279703..67280865hg38UCSC Ensembl
chr15:67572041..67573203hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381163
hg191163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2572n223
Supporting Variantsnssv18238960
Samples
Known GenesIQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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