A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001918



Internal ID18744449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180917614..180938869hg38UCSC Ensembl
Innerchr1:180886750..180908005hg19UCSC Ensembl
Innerchr1:179153373..179174628hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3821256
hg1921256
hg1821256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3483176
Samples
Known GenesKIAA1614
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001918
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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