A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028042



Internal ID19117260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..63071154hg38UCSC Ensembl
Innerchr7:61063962..62531532hg19UCSC Ensembl
Innerchr7:61067904..62168967hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381989918
hg191467571
hg181101064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6386n100
Supporting Variantsnssv3661554
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028042
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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