A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058763



Internal ID18801294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34130852..34196904hg38UCSC Ensembl
Innerchr19:34621757..34687809hg19UCSC Ensembl
Innerchr19:39313597..39379649hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3866053
hg1966053
hg1866053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3515n100
Supporting Variantsnssv3566587
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)nsv1058763
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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