A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013555



Internal ID19102773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117490138..117640926hg38UCSC Ensembl
Innerchr2:118247714..118398502hg19UCSC Ensembl
Innerchr2:117964184..118114972hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38150789
hg19150789
hg18150789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4060n100
Supporting Variantsnssv3729215
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013555
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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