A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007724



Internal ID19096943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6586380..6611657hg38UCSC Ensembl
Innerchr4:6588107..6613384hg19UCSC Ensembl
Innerchr4:6639008..6664285hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3825278
hg1925278
hg1825278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616183
Samples
Known GenesMAN2B2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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