A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575572



Internal ID20948643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38059774..38060745hg38UCSC Ensembl
chr8:37917292..37918263hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277894
Samples
Known GenesEIF4EBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575572
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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