A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556576



Internal ID20929647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26997047..26997580hg38UCSC Ensembl
chr9:26997045..26997578hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280408
Samples
Known GenesIFT74, LRRC19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556576
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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