A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150037



Internal ID15508999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8483291..8532981hg38UCSC Ensembl
Innerchr19:8548175..8597865hg19UCSC Ensembl
Innerchr19:8454175..8503865hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3849691
hg1949691
hg1849691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578559
Supporting Variants
Samples1782681247_A
Known GenesHNRNPM, MYO1F, PRAM1, ZNF414
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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