A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018170



Internal ID19107387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:50391536..50420134hg38UCSC Ensembl
Innerchr6:50359249..50387847hg19UCSC Ensembl
Innerchr6:50467208..50495806hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3828599
hg1928599
hg1828599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745482
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)nsv1018170
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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