A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527510



Internal ID22396896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266086..16266161hg38UCSC Ensembl
chr6:16266317..16266392hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7756n152
Supporting Variantsnssv14327564, nssv14327563, nssv14327561, nssv14327560, nssv14327562
SamplesHG00512, NA19238, NA19239, NA19240, HG00514
Known GenesGMPR
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527510
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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