A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2907520



Internal ID15390062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68053175..68129695hg38UCSC Ensembl
Innerchr4:68918893..68995413hg19UCSC Ensembl
Innerchr4:68601488..68678008hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3876521
hg1976521
hg1876521
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515010
Supporting Variants
SamplesNA19122
Known GenesLOC550113, SYT14L, TMPRSS11F
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2907520
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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