A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990150



Internal ID12637407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102717873..103146688hg38UCSC Ensembl
Innerchr7:102358320..102787135hg19UCSC Ensembl
Innerchr7:102145556..102574371hg18UCSC Ensembl
Innerchr7:101952271..102381086hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38428816
hg19428816
hg18428816
hg17428816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752138
Supporting Variants
SamplesSPC_61
Known GenesARMC10, FAM185A, FBXL13, LRRC17, NAPEPLD, RPL19P12
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990150
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer