A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014066



Internal ID19103286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119567451..119605792hg38UCSC Ensembl
Innerchr1:120110074..120148415hg19UCSC Ensembl
Innerchr1:119911597..119949938hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3838342
hg1938342
hg1838342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv302n100
Supporting Variantsnssv3496265
Samples
Known GenesHSD3BP4, LINC00622
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014066
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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