A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978499



Internal ID12635396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59096134..59135634hg38UCSC Ensembl
Innerchr10:60855894..60895394hg19UCSC Ensembl
Innerchr10:60525900..60565400hg18UCSC Ensembl
Innerchr10:60525900..60565400hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3839501
hg1939501
hg1839501
hg1739501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34715
Supporting Variants
SamplesNA19127
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978499
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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