A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049106



Internal ID19138325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99027593..99066806hg38UCSC Ensembl
Innerchr13:99679847..99719060hg19UCSC Ensembl
Innerchr13:98477848..98517061hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3839214
hg1939214
hg1839214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525524
Samples
Known GenesDOCK9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049106
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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