A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987526



Internal ID12977868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36276443..36313743hg38UCSC Ensembl
Innerchr14:36745649..36782949hg19UCSC Ensembl
Innerchr14:35815400..35852700hg18UCSC Ensembl
Innerchr14:35815400..35852700hg17UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3837301
hg1937301
hg1837301
hg1737301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751271
Supporting Variants
SamplesBEC_806
Known GenesMBIP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987526
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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