A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173985



Internal ID15854509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:194802203..194863360hg38UCSC Ensembl
Innerchr1:194771333..194832490hg19UCSC Ensembl
Innerchr1:193037956..193099113hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3861158
hg1961158
hg1861158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv548697
Supporting Variants
Samples1780862176_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173985
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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