A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036226



Internal ID19125445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91769467..91849030hg38UCSC Ensembl
Innerchr13:92421721..92501284hg19UCSC Ensembl
Innerchr13:91219722..91299285hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3879564
hg1979564
hg1879564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1729n100
Supporting Variantsnssv3525482
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)nsv1036226
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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