A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648169



Internal ID18599764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150777862..150933758hg38UCSC Ensembl
Innerchr5:150157424..150313320hg19UCSC Ensembl
Innerchr5:150137617..150293513hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38155897
hg19155897
hg18155897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021828
Supporting Variants
Samples
Known GenesIRGM, SMIM3, ZNF300, ZNF300P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648169
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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