A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039315



Internal ID19128534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102046039..102106184hg38UCSC Ensembl
Innerchr13:102698389..102758534hg19UCSC Ensembl
Innerchr13:101496390..101556535hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3860146
hg1960146
hg1860146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1733n100
Supporting Variantsnssv3525534
Samples
Known GenesFGF14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039315
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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