A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038914



Internal ID18781445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110207872..110537757hg38UCSC Ensembl
Innerchr13:110860219..111190104hg19UCSC Ensembl
Innerchr13:109658220..109988105hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38329886
hg19329886
hg18329886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713308
Samples
Known GenesCOL4A1, COL4A2, COL4A2-AS1, MIR8073, RAB20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038914
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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