A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030846



Internal ID19120065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15975716..15988500hg38UCSC Ensembl
Innerchr7:16015341..16028125hg19UCSC Ensembl
Innerchr7:15981866..15994650hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3812785
hg1912785
hg1812785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643189
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)nsv1030846
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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