A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv718457



Internal ID15665727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:85200587..85201925hg38UCSC Ensembl
Innerchr1:85666270..85667608hg19UCSC Ensembl
Innerchr1:85438858..85440196hg18UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381339
hg191339
hg181339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546709
Supporting Variants
Samples
Known GenesSYDE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv718457
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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