A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv736763



Internal ID16030719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210130974..210165052hg38UCSC Ensembl
Innerchr1:210304319..210338397hg19UCSC Ensembl
Innerchr1:208370942..208405020hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3834079
hg1934079
hg1834079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549105
Supporting Variants
Samples
Known GenesSYT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv736763
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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