A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19607



Internal ID15836031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50707853..50710900hg38UCSC Ensembl
Outerchr10:50706589..50736182hg38UCSC Ensembl
Innerchr10:52467613..52470660hg19UCSC Ensembl
Outerchr10:52466349..52495942hg19UCSC Ensembl
Innerchr10:52137619..52140666hg18UCSC Ensembl
Outerchr10:52136355..52165948hg18UCSC Ensembl
Innerchr10:52137619..52140666hg17UCSC Ensembl
Outerchr10:52136355..52165948hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3829594
hg1929594
hg1829594
hg1729594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8663
Supporting Variants
SamplesNA18563
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv19607
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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