A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571188



Internal ID20944259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15427533..15428001hg38UCSC Ensembl
chr9:15427531..15427999hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280209
Samples
Known GenesSNAPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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