A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv729719



Internal ID15676989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180781565..180786052hg38UCSC Ensembl
Innerchr1:180750701..180755188hg19UCSC Ensembl
Innerchr1:179017324..179021811hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg384488
hg194488
hg184488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548350
Supporting Variants
Samples
Known GenesXPR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv729719
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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