A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3468957



Internal ID18716436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8996436..9054032hg38UCSC Ensembl
Innerchr1:9056495..9114091hg19UCSC Ensembl
Innerchr1:8979082..9036678hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3857597
hg1957597
hg1857597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009990
Supporting Variants
Samples
Known GenesSLC2A5, SLC2A7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3468957
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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