A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984995



Internal ID12983856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:37276066..37380866hg38UCSC Ensembl
Innerchr10:37564994..37669794hg19UCSC Ensembl
Innerchr10:37605000..37709800hg18UCSC Ensembl
Innerchr10:37605000..37709800hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38104801
hg19104801
hg18104801
hg17104801
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)essv6984995
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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