A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002228



Internal ID19091445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105425049..105512224hg38UCSC Ensembl
Innerchr4:106346206..106433381hg19UCSC Ensembl
Innerchr4:106565655..106652830hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3887176
hg1987176
hg1887176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632406
Samples
Known GenesPPA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002228
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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