A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34257



Internal ID12643610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69499630hg38UCSC Ensembl
Innerchr9:72100051..72114546hg19UCSC Ensembl
Innerchr9:71289871..71304366hg18UCSC Ensembl
Innerchr9:69329605..69344100hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3814496
hg1914496
hg1814496
hg1714496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6980401, essv6980400, essv6987785
SamplesNA10831
Known GenesAPBA1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34257
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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