A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018854



Internal ID19108071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79691200..79775641hg38UCSC Ensembl
Innerchr7:79320516..79404957hg19UCSC Ensembl
Innerchr7:79158452..79242893hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3884442
hg1984442
hg1884442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6512n100
Supporting Variantsnssv3657187, nssv3657185, nssv3755405, nssv3755407, nssv3755406, nssv3657184, nssv3657186, nssv3755408
Samples
Known GenesMIR548M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018854
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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