A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27570



Internal ID15497514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84187008..84232476hg38UCSC Ensembl
Outerchr15:84186678..84233220hg38UCSC Ensembl
Innerchr15:84855760..84901228hg19UCSC Ensembl
Outerchr15:84855430..84901972hg19UCSC Ensembl
Innerchr15:82646764..82692232hg18UCSC Ensembl
Outerchr15:82646434..82692976hg18UCSC Ensembl
Innerchr15:82646764..82692232hg17UCSC Ensembl
Outerchr15:82646434..82692976hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3846543
hg1946543
hg1846543
hg1746543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9290
Supporting Variants
SamplesNA19221
Known GenesLOC388152, LOC440300, LOC642423
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)nssv27570
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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