A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015802



Internal ID19105020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88564353..88597603hg38UCSC Ensembl
Innerchr6:89274072..89307322hg19UCSC Ensembl
Innerchr6:89330791..89364041hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3833251
hg1933251
hg1833251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648946
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)nsv1015802
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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