A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561173



Internal ID20934244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47363283..48194139hg38UCSC Ensembl
chr7:47402881..48233736hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38830857
hg19830856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274515
Samples
Known GenesABCA13, C7orf57, C7orf65, C7orf69, HUS1, LINC00525, LOC101929086, PKD1L1, SUN3, TNS3, UPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561173
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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