A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568444



Internal ID20941515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56041231..56041854hg38UCSC Ensembl
chr7:56108924..56109547hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274680
Samples
Known GenesPSPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568444
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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