A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523976



Internal ID18822257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57138666..57202423hg38UCSC Ensembl
Innerchr13:57712800..57776557hg19UCSC Ensembl
Innerchr13:56610801..56674558hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3863758
hg1963758
hg1863758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053237
Supporting Variants
Samples
Known GenesPRR20A, PRR20B, PRR20C, PRR20D, PRR20E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523976
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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