A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150029



Internal ID15533911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6901880..7105125hg38UCSC Ensembl
Innerchr19:6901891..7105136hg19UCSC Ensembl
Innerchr19:6852891..7056136hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38203246
hg19203246
hg18203246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578468
Supporting Variants
SamplesNINDS_231
Known GenesEMR1, EMR4P, FLJ25758, MBD3L2, MBD3L3, MBD3L4, MBD3L5, ZNF557
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150029
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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