A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751762



Internal ID12638628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46135838..46286690hg38UCSC Ensembl
Innerchr17:44213204..44364056hg19UCSC Ensembl
Innerchr17:41568981..41719833hg18UCSC Ensembl
Innerchr17:41568981..41719833hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38150853
hg19150853
hg18150853
hg17150853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv131e55
Supporting Variantsessv6980309, essv6989164
SamplesNA07029
Known GenesKANSL1, KANSL1-AS1, LOC644172
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)esv2751762
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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