A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018182



Internal ID19107399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119512444..119545638hg38UCSC Ensembl
Innerchr6:119833609..119866803hg19UCSC Ensembl
Innerchr6:119875308..119908502hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3833195
hg1933195
hg1833195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654335
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)nsv1018182
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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