A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723234



Internal ID18674829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76317786..77170410hg38UCSC Ensembl
Innerchr18:74029741..74882366hg19UCSC Ensembl
Innerchr18:72158729..73011354hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38852625
hg19852626
hg18852626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063632
Supporting Variants
Samples
Known GenesFLJ44313, LINC00908, LOC100131655, MBP, ZNF236, ZNF516
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723234
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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