A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577385



Internal ID16364794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69016897..69088271hg38UCSC Ensembl
Innerchr18:66684134..66755508hg19UCSC Ensembl
Innerchr18:64835114..64906488hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3871375
hg1971375
hg1871375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6023n54
Supporting Variantsnssv886499, nssv886496, nssv886495, nssv886493, nssv886503, nssv886502, nssv886494, nssv886500, nssv886497, nssv886498, nssv886501
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577385
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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