A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559908



Internal ID20932979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129092553..129093173hg38UCSC Ensembl
chr7:128732607..128733227hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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