A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038122



Internal ID18780653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:67020323..67061488hg38UCSC Ensembl
Innerchr14:67487040..67528205hg19UCSC Ensembl
Innerchr14:66556793..66597958hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3841166
hg1941166
hg1841166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531102
Samples
Known GenesGPHN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038122
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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