A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985427



Internal ID12635552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99826272..100046272hg38UCSC Ensembl
Innerchr15:100366477..100586477hg19UCSC Ensembl
Innerchr15:98184000..98404000hg18UCSC Ensembl
Innerchr15:98184000..98404000hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38220001
hg19220001
hg18220001
hg17220001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34620
Supporting Variants
SamplesNA19141
Known GenesADAMTS17
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985427
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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