A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064685



Internal ID19153904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76490331..76542981hg38UCSC Ensembl
Innerchr18:74202287..74254938hg19UCSC Ensembl
Innerchr18:72331275..72383926hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3852651
hg1952652
hg1852652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563030
Samples
Known GenesFLJ44313, LINC00908, ZNF516
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064685
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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