A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981930



Internal ID12627477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14599395..14624195hg38UCSC Ensembl
Innerchr10:14641394..14666194hg19UCSC Ensembl
Innerchr10:14681400..14706200hg18UCSC Ensembl
Innerchr10:14681400..14706200hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3824801
hg1924801
hg1824801
hg1724801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750884
Supporting Variants
SamplesBEC_502
Known GenesFAM107B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981930
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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