A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173221



Internal ID15873579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:168803155..168856794hg38UCSC Ensembl
Innerchr1:168772393..168826032hg19UCSC Ensembl
Innerchr1:167039017..167092656hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3853640
hg1953640
hg1853640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548145
Supporting Variants
SamplesHGDP00251
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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