A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038089



Internal ID18780620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110577170..110622476hg38UCSC Ensembl
Innerchr13:111229517..111274823hg19UCSC Ensembl
Innerchr13:110027518..110072824hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3845307
hg1945307
hg1845307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525582
Samples
Known GenesCARKD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038089
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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