A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056800



Internal ID19146019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27778026..27799426hg38UCSC Ensembl
Innerchr18:25357990..25379390hg19UCSC Ensembl
Innerchr18:23611988..23633388hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3821401
hg1921401
hg1821401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3327n100
Supporting Variantsnssv3564142
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)nsv1056800
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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