A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009302



Internal ID19098520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101413915..101489736hg38UCSC Ensembl
Innerchr4:102335072..102410893hg19UCSC Ensembl
Innerchr4:102554095..102629916hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3875822
hg1975822
hg1875822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3631012
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009302
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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