A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982181



Internal ID12973316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87287299..87326577hg38UCSC Ensembl
Innerchr15:87830530..87869808hg19UCSC Ensembl
Innerchr15:85631534..85670812hg18UCSC Ensembl
Innerchr15:85631534..85670812hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3839279
hg1939279
hg1839279
hg1739279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751539
Supporting Variants
SamplesBEC_400
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982181
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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