A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041777



Internal ID19130996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42503822..42655964hg38UCSC Ensembl
Innerchr14:42973025..43125167hg19UCSC Ensembl
Innerchr14:42042775..42194917hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38152143
hg19152143
hg18152143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1888n100
Supporting Variantsnssv3530214
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)nsv1041777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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