A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3487288



Internal ID19074929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:184694764..184762081hg38UCSC Ensembl
Innerchr1:184663898..184731215hg19UCSC Ensembl
Innerchr1:182930521..182997838hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3867318
hg1967318
hg1867318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009529
Supporting Variants
Samples
Known GenesEDEM3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3487288
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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