A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013126



Internal ID19102344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119456171..119494314hg38UCSC Ensembl
Innerchr1:119998794..120036937hg19UCSC Ensembl
Innerchr1:119800317..119838460hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3838144
hg1938144
hg1838144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv299n100
Supporting Variantsnssv3496643
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)nsv1013126
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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