A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041168



Internal ID19130387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91409803..91649607hg38UCSC Ensembl
Innerchr13:92062057..92301861hg19UCSC Ensembl
Innerchr13:90860058..91099862hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38239805
hg19239805
hg18239805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525479, nssv3713270, nssv3525478, nssv3713272, nssv3525480, nssv3713271
Samples
Known GenesGPC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041168
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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