A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531089



Internal ID18482684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66518523..66574905hg38UCSC Ensembl
Innerchr14:66985241..67041623hg19UCSC Ensembl
Innerchr14:66054994..66111376hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3856383
hg1956383
hg1856383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040383
Supporting Variants
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)nssv3531089
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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