A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037719



Internal ID19126938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37029636..37077154hg38UCSC Ensembl
Innerchr14:37498841..37546359hg19UCSC Ensembl
Innerchr14:36568592..36616110hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3847519
hg1947519
hg1847519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1870n100
Supporting Variantsnssv3528625, nssv3528624, nssv3712282
Samples
Known GenesSLC25A21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037719
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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