A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3700295



Internal ID18998576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18020216..18047245hg38UCSC Ensembl
Innerchr1:18346710..18373739hg19UCSC Ensembl
Innerchr1:18219297..18246326hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3827030
hg1927030
hg1827030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014415
Supporting Variants
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)nssv3700295
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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