A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529174



Internal ID22398567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064898..72065202hg38UCSC Ensembl
chr10:73824656..73824960hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353441, nssv14353443, nssv14353442, nssv14353444
SamplesNA19239, HG00731, NA19240, HG00733
Known GenesSPOCK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529174
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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