A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563519



Internal ID20936590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118241161..118241537hg38UCSC Ensembl
chr7:117881215..117881591hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272276
Samples
Known GenesANKRD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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