A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984039



Internal ID12977587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19798858..20118651hg38UCSC Ensembl
Innerchr4:19800481..20120274hg19UCSC Ensembl
Innerchr4:19409579..19729372hg18UCSC Ensembl
Innerchr4:19476750..19796543hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38319794
hg19319794
hg18319794
hg17319794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752044
Supporting Variants
SamplesBEC_758
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984039
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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