A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635382



Internal ID18586977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:169856351..169992747hg38UCSC Ensembl
Innerchr4:170777502..170913898hg19UCSC Ensembl
Innerchr4:171014077..171150473hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38136397
hg19136397
hg18136397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020188
Supporting Variants
Samples
Known GenesLOC100506085, MFAP3L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635382
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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