A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037586



Internal ID19126805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62192490..62242057hg38UCSC Ensembl
Innerchr14:62659208..62708775hg19UCSC Ensembl
Innerchr14:61728961..61778528hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3849568
hg1949568
hg1849568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1924n100
Supporting Variantsnssv3531051
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)nsv1037586
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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