A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701989



Internal ID15438641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:97048899..97135275hg38UCSC Ensembl
Innerchr3:96767743..96854119hg19UCSC Ensembl
Innerchr3:98250433..98336809hg18UCSC Ensembl
Innerchr3:98250433..98336809hg17UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3886377
hg1986377
hg1886377
hg1786377
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525805
Supporting Variants
Samples
Known GenesEPHA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701989
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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