A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986366



Internal ID12628290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44715246..44785046hg38UCSC Ensembl
Innerchr10:45210694..45280494hg19UCSC Ensembl
Innerchr10:44530700..44600500hg18UCSC Ensembl
Innerchr10:44530700..44600500hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3869801
hg1969801
hg1869801
hg1769801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750895
Supporting Variants
SamplesBEC_554
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986366
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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