A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036021



Internal ID19125240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40476459..40565454hg38UCSC Ensembl
Innerchr14:40945663..41034659hg19UCSC Ensembl
Innerchr14:40015413..40104409hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3888996
hg1988997
hg1888997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1879n100
Supporting Variantsnssv3712293
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)nsv1036021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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