A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048157



Internal ID19137376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97661651..97681388hg38UCSC Ensembl
Innerchr14:98127988..98147725hg19UCSC Ensembl
Innerchr14:97197741..97217478hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3819738
hg1919738
hg1819738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532636
Samples
Known GenesLOC100129345
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048157
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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