A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034059



Internal ID19123281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12302923..12328192hg38UCSC Ensembl
Innerchr7:12342549..12367818hg19UCSC Ensembl
Innerchr7:12309074..12334343hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3825270
hg1925270
hg1825270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752890
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)nsv1034059
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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