A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990129



Internal ID12983914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19478137..19562337hg38UCSC Ensembl
Innerchr7:19517760..19601960hg19UCSC Ensembl
Innerchr7:19484285..19568485hg18UCSC Ensembl
Innerchr7:19291000..19375200hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3884201
hg1984201
hg1884201
hg1784201
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990129
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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