A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055949



Internal ID19145168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27290371hg38UCSC Ensembl
Innerchr19:27747981..27781279hg19UCSC Ensembl
Innerchr19:32439821..32473119hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3833299
hg1933299
hg1833299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3493n100
Supporting Variantsnssv3570789
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055949
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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