A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562319



Internal ID20935390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8246756..8247455hg38UCSC Ensembl
chr7:8286386..8287085hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276743
Samples
Known GenesICA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562319
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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