A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581688



Internal ID20954759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74127701..74128313hg38UCSC Ensembl
chr10:75887459..75888071hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv813n223
Supporting Variantsnssv18219559
Samples
Known GenesAP3M1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581688
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