A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043801



Internal ID19133020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35023859..35070193hg38UCSC Ensembl
Innerchr14:35493065..35539399hg19UCSC Ensembl
Innerchr14:34562816..34609150hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3846335
hg1946335
hg1846335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528612
Samples
Known GenesFAM177A1, SRP54
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043801
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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