A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033466



Internal ID19122687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93865383..93914903hg38UCSC Ensembl
Innerchr5:93201089..93250608hg19UCSC Ensembl
Innerchr5:93226845..93276364hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3849521
hg1949520
hg1849520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639934, nssv3639935
Samples
Known GenesFAM172A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033466
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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