A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056217



Internal ID19145436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39098609..39243742hg38UCSC Ensembl
Innerchr18:36678573..36823706hg19UCSC Ensembl
Innerchr18:34932571..35077704hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38145134
hg19145134
hg18145134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564216
Samples
Known GenesLINC00669
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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