A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2908487



Internal ID15754915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56674005..56678077hg38UCSC Ensembl
Innerchr4:57540171..57544243hg19UCSC Ensembl
Innerchr4:57234928..57239000hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg384073
hg194073
hg184073
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514214
Supporting Variants
SamplesNA19184
Known GenesHOPX
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2908487
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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