A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989873



Internal ID12630647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34484566..34685612hg38UCSC Ensembl
Innerchr15:34776767..34977813hg19UCSC Ensembl
Innerchr15:32564059..32765105hg18UCSC Ensembl
Innerchr15:32564059..32765105hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38201047
hg19201047
hg18201047
hg17201047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751533
Supporting Variants
SamplesBEC_728
Known GenesGOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989873
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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