A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556280



Internal ID20929351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127631349..127631934hg38UCSC Ensembl
chr7:127271403..127271988hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556280
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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