A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558588



Internal ID20931659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44843087..44843862hg38UCSC Ensembl
chr7:44882686..44883461hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276008
Samples
Known GenesH2AFV
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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