A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639554



Internal ID18591149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134003215..134267621hg38UCSC Ensembl
Innerchr4:134924370..135188776hg19UCSC Ensembl
Innerchr4:135143820..135408226hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38264407
hg19264407
hg18264407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028039
Supporting Variants
Samples
Known GenesPABPC4L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639554
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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