A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161363



Internal ID8252711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:94019946..94326277hg38UCSC Ensembl
Innerchr7:93649258..93955589hg19UCSC Ensembl
Innerchr7:93487194..93793525hg18UCSC Ensembl
Innerchr7:93293909..93600240hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38306332
hg19306332
hg18306332
hg17306332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422226
Supporting Variants
SamplesND01670
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161363
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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