A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555785



Internal ID20928856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52428592..52429129hg38UCSC Ensembl
chr7:52496288..52496825hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274600
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555785
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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