A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027311



Internal ID19116530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:138757455..138790572hg38UCSC Ensembl
Innerchr4:139678609..139711726hg19UCSC Ensembl
Innerchr4:139898059..139931176hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3833118
hg1933118
hg1833118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641179
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)nsv1027311
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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