A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527925



Internal ID22397311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99535434..99535528hg38UCSC Ensembl
chr10:101295191..101295285hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1027n152
Supporting Variantsnssv14352906, nssv14352909, nssv14352908, nssv14352905, nssv14352907
SamplesHG00512, NA19238, NA19239, NA19240, HG00733
Known GenesNKX2-3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527925
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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