A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568983



Internal ID20942054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140460149..140460594hg38UCSC Ensembl
chr7:140159949..140160394hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274447
Samples
Known GenesMKRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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