A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579423



Internal ID16020146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35730150..35792945hg38UCSC Ensembl
Innerchr19:36221051..36283847hg19UCSC Ensembl
Innerchr19:40912891..40975687hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3862796
hg1962797
hg1862797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898983
Samples
Known GenesARHGAP33, C19orf55, HSPB6, IGFLR1, KMT2B, LIN37, LOC644050, PSENEN, U2AF1L4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579423
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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