A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150026



Internal ID15881079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6895855..7000390hg38UCSC Ensembl
Innerchr19:6895866..7000401hg19UCSC Ensembl
Innerchr19:6846866..6951401hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38104536
hg19104536
hg18104536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578464
Supporting Variants
SamplesNINDS_66
Known GenesEMR1, EMR4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150026
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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