A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067311



Internal ID18809842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:63818011..66637685hg38UCSC Ensembl
Innerchr18:61485245..64304922hg19UCSC Ensembl
Innerchr18:59636225..62455902hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg382819675
hg192819678
hg182819678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565627
Samples
Known GenesCDH19, CDH7, HMSD, LINC00305, LOC284294, LOC400654, SERPINB10, SERPINB2, SERPINB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067311
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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