A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037815



Internal ID18780346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92306849..92399755hg38UCSC Ensembl
Innerchr13:92959102..93052008hg19UCSC Ensembl
Innerchr13:91757103..91850009hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3892907
hg1992907
hg1892907
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1730n100
Supporting Variantsnssv3713275
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)nsv1037815
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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