A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031064



Internal ID19120285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11867944..11898981hg38UCSC Ensembl
Innerchr7:11907570..11938607hg19UCSC Ensembl
Innerchr7:11874095..11905132hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3831038
hg1931038
hg1831038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642951
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)nsv1031064
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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