A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028562



Internal ID19117780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142049538..142084684hg38UCSC Ensembl
Innerchr7:141749338..141784484hg19UCSC Ensembl
Innerchr7:141395807..141430953hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3835147
hg1935147
hg1835147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664289
Samples
Known GenesMGAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028562
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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