A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3704811



Internal ID19003092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:164104484..164162308hg38UCSC Ensembl
Innerchr1:164073721..164131545hg19UCSC Ensembl
Innerchr1:162340345..162398169hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3857825
hg1957825
hg1857825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006601
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)nssv3704811
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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