A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568977



Internal ID20942048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129339919..129340485hg38UCSC Ensembl
chr7:128979760..128980326hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273062
Samples
Known GenesAHCYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568977
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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