A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581931



Internal ID20955002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41235246..41236542hg38UCSC Ensembl
chr15:41527444..41528740hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381297
hg191297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238314
Samples
Known GenesCHP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581931
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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