A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556168



Internal ID20929239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2413740..2472703hg38UCSC Ensembl
chr7:2453375..2512338hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3858964
hg1958964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272735
Samples
Known GenesCHST12, LOC101927181
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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