A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985828



Internal ID12637412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102850602..103146602hg38UCSC Ensembl
Innerchr7:102491049..102787049hg19UCSC Ensembl
Innerchr7:102278285..102574285hg18UCSC Ensembl
Innerchr7:102085000..102381000hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38296001
hg19296001
hg18296001
hg17296001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752138
Supporting Variants
SamplesSPC_61
Known GenesARMC10, FBXL13, LRRC17, NAPEPLD, RPL19P12
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985828
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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