A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056784



Internal ID19146003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78622921..78681382hg38UCSC Ensembl
Innerchr18:76382921..76441382hg19UCSC Ensembl
Innerchr18:74483909..74542370hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3858462
hg1958462
hg1858462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3411n100
Supporting Variantsnssv3563060
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)nsv1056784
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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