A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722718



Internal ID19020999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58943769..59007329hg38UCSC Ensembl
Innerchr16:58977673..59041233hg19UCSC Ensembl
Innerchr16:57535174..57598734hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3863561
hg1963561
hg1863561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055767
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)nssv3722718
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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