A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027622



Internal ID19116841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:174759178..174794919hg38UCSC Ensembl
Innerchr4:175680329..175716070hg19UCSC Ensembl
Innerchr4:175916904..175952645hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3835742
hg1935742
hg1835742
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744520
Samples
Known GenesGLRA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027622
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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