A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035546



Internal ID19124765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:56714061..56731228hg38UCSC Ensembl
Innerchr14:57180779..57197946hg19UCSC Ensembl
Innerchr14:56250532..56267699hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3817168
hg1917168
hg1817168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1923n100
Supporting Variantsnssv3531037, nssv3531036
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)nsv1035546
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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