A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752141



Internal ID12985693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111147914..111473535hg38UCSC Ensembl
Innerchr7:110787970..111113591hg19UCSC Ensembl
Innerchr7:110575206..110900827hg18UCSC Ensembl
Innerchr7:110381921..110707542hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38325622
hg19325622
hg18325622
hg17325622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6985210, essv6985211
SamplesSPC_124
Known GenesIMMP2L
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752141
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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