A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173014



Internal ID15855656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70415034..70456677hg38UCSC Ensembl
Innerchr1:70880717..70922360hg19UCSC Ensembl
Innerchr1:70653305..70694948hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3841644
hg1941644
hg1841644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546456
Supporting Variants
Samples1782681216_A
Known GenesCTH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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