A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563275



Internal ID20936346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142782774..143009946hg38UCSC Ensembl
chr7:142490584..142707033hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38227173
hg19216450
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274505
Samples
Known GenesC7orf34, EPHB6, KEL, TRPV5, TRPV6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563275
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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