A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995929



Internal ID15943199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38804398..38873181hg38UCSC Ensembl
Innerchr4:38806019..38874802hg19UCSC Ensembl
Innerchr4:38482414..38551197hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3868784
hg1968784
hg1868784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594010
Supporting Variants
Samples
Known GenesFAM114A1, MIR574, TLR1, TLR6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv995929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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