A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023249



Internal ID18765781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133946159..134064530hg38UCSC Ensembl
Innerchr4:134867314..134985685hg19UCSC Ensembl
Innerchr4:135086764..135205135hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38118372
hg19118372
hg18118372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639535, nssv3639536, nssv3743110
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)nsv1023249
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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