A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985715



Internal ID12983910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19473937..19570537hg38UCSC Ensembl
Innerchr7:19513560..19610160hg19UCSC Ensembl
Innerchr7:19480085..19576685hg18UCSC Ensembl
Innerchr7:19286800..19383400hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3896601
hg1996601
hg1896601
hg1796601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752153
Supporting Variants
SamplesSPC_36
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985715
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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