A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056459



Internal ID18798990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48251299..48261624hg38UCSC Ensembl
Innerchr19:48754556..48764881hg19UCSC Ensembl
Innerchr19:53446368..53456693hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3810326
hg1910326
hg1810326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3574963
Samples
Known GenesCARD8, LOC100505812
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056459
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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