A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989066



Internal ID12632953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82687507..82784743hg38UCSC Ensembl
Innerchr15:83356259..83453495hg19UCSC Ensembl
Innerchr15:81153313..81250549hg18UCSC Ensembl
Innerchr15:81153313..81250549hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3897237
hg1997237
hg1897237
hg1797237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34318
Supporting Variants
SamplesNA12891
Known GenesAP3B2, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989066
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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