A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3637095



Internal ID18588690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38520095..38544303hg38UCSC Ensembl
Innerchr5:38520197..38544405hg19UCSC Ensembl
Innerchr5:38555954..38580162hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3824209
hg1924209
hg1824209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021616
Supporting Variants
Samples
Known GenesLIFR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3637095
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer