A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3494779



Internal ID18735734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:233567984..233611780hg38UCSC Ensembl
Innerchr1:233703730..233747526hg19UCSC Ensembl
Innerchr1:231770353..231814149hg18UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3843797
hg1943797
hg1843797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008006
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)nssv3494779
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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