A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044114



Internal ID19133333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62192490..62238946hg38UCSC Ensembl
Innerchr14:62659208..62705664hg19UCSC Ensembl
Innerchr14:61728961..61775417hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3846457
hg1946457
hg1846457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1924n100
Supporting Variantsnssv3531050
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)nsv1044114
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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