A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576543



Internal ID16363952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14949002..15178341hg38UCSC Ensembl
Innerchr18:14949001..15178340hg19UCSC Ensembl
Innerchr18:14939001..15168340hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38229340
hg19229340
hg18229340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878461
Samples
Known GenesLOC400644
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576543
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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