A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539337



Internal ID20912635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15916595..15917064hg38UCSC Ensembl
chr1:16243090..16243559hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247791
Samples
Known GenesSPEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539337
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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