A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983021



Internal ID12974699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12541641..12580847hg38UCSC Ensembl
Innerchr16:12635498..12674704hg19UCSC Ensembl
Innerchr16:12542999..12582205hg18UCSC Ensembl
Innerchr16:12542999..12582205hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3839207
hg1939207
hg1839207
hg1739207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751546
Supporting Variants
SamplesBEC_535
Known GenesSNX29
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983021
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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