A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525582



Internal ID18477177
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 StatusS
Merged Variantsnsv1038089
Supporting Variants
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)nssv3525582
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer