A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064154



Internal ID19153373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34620772..34661555hg38UCSC Ensembl
Innerchr19:35111677..35152460hg19UCSC Ensembl
Innerchr19:39803517..39844300hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3840784
hg1940784
hg1840784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566589
Samples
Known GenesSCGB2B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064154
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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