A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008703



Internal ID19097920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:60394683..60464169hg38UCSC Ensembl
Innerchr1:60860355..60929841hg19UCSC Ensembl
Innerchr1:60632943..60702429hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3869487
hg1969487
hg1869487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482166
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)nsv1008703
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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