A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038491



Internal ID19127710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14968554..15015784hg38UCSC Ensembl
Innerchr10:15010553..15057783hg19UCSC Ensembl
Innerchr10:15050559..15097789hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3847231
hg1947231
hg1847231
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707697
Samples
Known GenesMEIG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038491
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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