A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526307



Internal ID22395687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150084360..150084468hg38UCSC Ensembl
chr5:149463923..149464031hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7563n152
Supporting Variantsnssv14324319, nssv14324317, nssv14324314, nssv14324320, nssv14324321, nssv14324318, nssv14324315, nssv14324316
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00514
Known GenesCSF1R
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526307
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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