A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571515



Internal ID20944586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73610939..73611582hg38UCSC Ensembl
chr7:73025269..73025912hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276496
Samples
Known GenesMLXIPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571515
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer