A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062566



Internal ID18805097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48236633..48261203hg38UCSC Ensembl
Innerchr19:48739890..48764460hg19UCSC Ensembl
Innerchr19:53431702..53456272hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3824571
hg1924571
hg1824571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3615n100
Supporting Variantsnssv3574950
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)nsv1062566
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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