A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056566



Internal ID18799097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74422691..74448490hg38UCSC Ensembl
Innerchr16:74456589..74482388hg19UCSC Ensembl
Innerchr16:73014090..73039889hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg3825800
hg1925800
hg1825800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559576
Samples
Known GenesGLG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056566
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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