A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057179



Internal ID19146398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:63646569..63679645hg38UCSC Ensembl
Innerchr18:61313803..61346879hg19UCSC Ensembl
Innerchr18:59464783..59497859hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3833077
hg1933077
hg1833077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565626
Samples
Known GenesSERPINB3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057179
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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