A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645909



Internal ID18944190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103145965..103204665hg38UCSC Ensembl
Innerchr5:102481669..102540366hg19UCSC Ensembl
Innerchr5:102509568..102568265hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3858701
hg1958698
hg1858698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020598
Supporting Variants
Samples
Known GenesPPIP5K2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3645909
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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