A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878370



Internal ID16172326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12657196..12658044hg38UCSC Ensembl
Innerchr18:12657195..12658043hg19UCSC Ensembl
Innerchr18:12647195..12648043hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38849
hg19849
hg18849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576500
Supporting Variants
Samples
Known GenesSPIRE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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