A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990058



Internal ID12983870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37276059..37380855hg38UCSC Ensembl
Innerchr10:37564987..37669783hg19UCSC Ensembl
Innerchr10:37604993..37709789hg18UCSC Ensembl
Innerchr10:37604993..37709789hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38104797
hg19104797
hg18104797
hg17104797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750892
Supporting Variants
SamplesSPC_3
Known GenesLINC00993
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990058
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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