A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532574



Internal ID18484169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87933909..87956225hg38UCSC Ensembl
Innerchr14:88400253..88422569hg19UCSC Ensembl
Innerchr14:87470006..87492322hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3822317
hg1922317
hg1822317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045768
Supporting Variants
Samples
Known GenesGALC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3532574
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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