A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011037



Internal ID19100254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:221583184..221636210hg38UCSC Ensembl
Innerchr1:221756526..221809552hg19UCSC Ensembl
Innerchr1:219823149..219876175hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3853027
hg1953027
hg1853027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3494268
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)nsv1011037
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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