A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066767



Internal ID19155986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:58255047..58271707hg38UCSC Ensembl
Innerchr18:55922279..55938939hg19UCSC Ensembl
Innerchr18:54073259..54089919hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3816661
hg1916661
hg1816661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3361n100
Supporting Variantsnssv3565476, nssv3726082
Samples
Known GenesNEDD4L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066767
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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