A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007085



Internal ID19096303
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 StatusM
Merged Variantsdgv151n100
Supporting Variantsnssv3468287, nssv3469741
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)nsv1007085
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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