A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036896



Internal ID19126115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20893865..20951442hg38UCSC Ensembl
Innerchr14:21362024..21419601hg19UCSC Ensembl
Innerchr14:20431864..20489441hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3857578
hg1957578
hg1857578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1802n100
Supporting Variantsnssv3531983, nssv3531971, nssv3531980, nssv3531979, nssv3531976, nssv3531978, nssv3531982, nssv3531974, nssv3531975, nssv3531977, nssv3531981, nssv3531973, nssv3531972
Samples
Known GenesECRP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036896
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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