A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045395



Internal ID19134614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92596203..92671016hg38UCSC Ensembl
Innerchr13:93248456..93323269hg19UCSC Ensembl
Innerchr13:92046457..92121270hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3874814
hg1974814
hg1874814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713276
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)nsv1045395
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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