A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3742880



Internal ID18694475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87318188..87685333hg38UCSC Ensembl
Innerchr4:88239340..88606485hg19UCSC Ensembl
Innerchr4:88458364..88825509hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38367146
hg19367146
hg18367146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002789
Supporting Variants
Samples
Known GenesDMP1, DSPP, HSD17B11, HSD17B13, NUDT9, SPARCL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3742880
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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