A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469741



Internal ID19063544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38546966..38575751hg38UCSC Ensembl
Innerchr1:39012638..39041423hg19UCSC Ensembl
Innerchr1:38785225..38814010hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3828786
hg1928786
hg1828786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007085
Supporting Variants
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)nssv3469741
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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