A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056545



Internal ID19145764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78622921..78666068hg38UCSC Ensembl
Innerchr18:76382921..76426068hg19UCSC Ensembl
Innerchr18:74483909..74527056hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3843148
hg1943148
hg1843148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3411n100
Supporting Variantsnssv3563058, nssv3563057, nssv3563059
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)nsv1056545
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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