A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22246



Internal ID15488932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84209558..84231304hg38UCSC Ensembl
Outerchr15:84203870..84231798hg38UCSC Ensembl
Innerchr15:84878310..84900056hg19UCSC Ensembl
Outerchr15:84872622..84900550hg19UCSC Ensembl
Innerchr15:82669314..82691060hg18UCSC Ensembl
Outerchr15:82663626..82691554hg18UCSC Ensembl
Innerchr15:82669314..82691060hg17UCSC Ensembl
Outerchr15:82663626..82691554hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3827929
hg1927929
hg1827929
hg1727929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9290
Supporting Variants
SamplesNA18552
Known GenesLOC388152, LOC440300
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)nssv22246
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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