A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639938



Internal ID18938219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93906905..93947291hg38UCSC Ensembl
Innerchr5:93242611..93282996hg19UCSC Ensembl
Innerchr5:93268367..93308752hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3840387
hg1940386
hg1840386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030870
Supporting Variants
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)nssv3639938
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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