A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009390



Internal ID19098608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236953272..236969573hg38UCSC Ensembl
Innerchr1:237116572..237132873hg19UCSC Ensembl
Innerchr1:235183195..235199496hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3816302
hg1916302
hg1816302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487154
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)nsv1009390
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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