A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045902



Internal ID19135121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63688137..63793857hg38UCSC Ensembl
Innerchr13:64262270..64367990hg19UCSC Ensembl
Innerchr13:63160271..63265991hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38105721
hg19105721
hg18105721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1686n100
Supporting Variantsnssv3526623, nssv3711777, nssv3711778, nssv3711775, nssv3711776, nssv3526621, nssv3526620, nssv3526622, nssv3526619
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045902
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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