A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998118



Internal ID19157655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36819990..36848132hg38UCSC Ensembl
Innerchr3:36861481..36889623hg19UCSC Ensembl
Innerchr3:36836485..36864627hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3828143
hg1928143
hg1828143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589672, nssv3589673, nssv3589674
Samples
Known GenesTRANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998118
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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