A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999203



Internal ID19158739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48643870..48733495hg38UCSC Ensembl
Innerchr4:48645887..48735512hg19UCSC Ensembl
Innerchr4:48340644..48430269hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3889626
hg1989626
hg1889626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625138
Samples
Known GenesFRYL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999203
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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