A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989285



Internal ID12627772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28724519..30026109hg38UCSC Ensembl
Innerchr15:28969665..30318312hg19UCSC Ensembl
Innerchr15:26768706..28105604hg18UCSC Ensembl
Innerchr15:26768706..28105604hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381301591
hg191348648
hg181336899
hg171336899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751526
Supporting Variants
SamplesBEC_521
Known GenesAPBA2, FAM189A1, GOLGA6L7P, LOC100289656, LOC646278, NDNL2, TJP1, WHAMMP2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989285
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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