A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011721



Internal ID19100939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:119572662..119606894hg38UCSC Ensembl
Innerchr1:120115285..120149517hg19UCSC Ensembl
Innerchr1:119916808..119951040hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3834233
hg1934233
hg1834233
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv303n100
Supporting Variantsnssv3491739, nssv3496896
Samples
Known GenesLINC00622
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011721
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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