A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981712



Internal ID12625897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9280561..10381631hg38UCSC Ensembl
Innerchr10:9322524..10423594hg19UCSC Ensembl
Innerchr10:9362530..10463600hg18UCSC Ensembl
Innerchr10:9362530..10463600hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381101071
hg191101071
hg181101071
hg171101071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750976
Supporting Variants
SamplesBEC_328
Known GenesLINC00709
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981712
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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