A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8604



Internal ID15499830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13015229..13019500hg38UCSC Ensembl
Outerchr10:13057229..13061500hg19UCSC Ensembl
Outerchr10:13097235..13101506hg18UCSC Ensembl
Outerchr10:13097235..13101506hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384272
hg194272
hg184272
hg174272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124
SamplesNA10839
Known GenesCCDC3
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)nsv8604
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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