A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064600



Internal ID18807131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34866434..34915441hg38UCSC Ensembl
Innerchr19:35357338..35406345hg19UCSC Ensembl
Innerchr19:40049178..40098185hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3849008
hg1949008
hg1849008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724356
Samples
Known GenesLINC00904
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064600
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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