A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057380



Internal ID18799911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34122371..34196904hg38UCSC Ensembl
Innerchr19:34613276..34687809hg19UCSC Ensembl
Innerchr19:39305116..39379649hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3874534
hg1974534
hg1874534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3515n100
Supporting Variantsnssv3566586
Samples
Known GenesLSM14A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057380
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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