A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027157



Internal ID19116376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:138344398..138381762hg38UCSC Ensembl
Innerchr4:139265552..139302916hg19UCSC Ensembl
Innerchr4:139485002..139522366hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3837365
hg1937365
hg1837365
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641178
Samples
Known GenesLINC00499
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027157
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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