A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035695



Internal ID18778226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:71857102..71916893hg38UCSC Ensembl
Innerchr14:72323819..72383610hg19UCSC Ensembl
Innerchr14:71393572..71453363hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3859792
hg1959792
hg1859792
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531127
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)nsv1035695
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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