A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984158



Internal ID12631102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21608949..21728953hg38UCSC Ensembl
Innerchr16:21620270..21740274hg19UCSC Ensembl
Innerchr16:21527771..21647775hg18UCSC Ensembl
Innerchr16:21527771..21647775hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38120005
hg19120005
hg18120005
hg17120005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751553
Supporting Variants
SamplesBEC_792
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984158
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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