A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619854



Internal ID18918135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16336568..16373541hg38UCSC Ensembl
Innerchr4:16338191..16375164hg19UCSC Ensembl
Innerchr4:15947289..15984262hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3836974
hg1936974
hg1836974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000106
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3619854
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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