A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516782



Internal ID15097389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143095565..143184447hg38UCSC Ensembl
Innerchr7:142792658..142881540hg19UCSC Ensembl
Innerchr7:142502780..142591662hg18UCSC Ensembl
Innerchr7:142309495..142398377hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3888883
hg1988883
hg1888883
hg1788883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv432n21
Supporting Variantsnssv692159, nssv681960, nssv674379, nssv660293, nssv670971, nssv660421, nssv673262, nssv691466, nssv670829, nssv659315, nssv677825, nssv672250, nssv657192, nssv674941, nssv690294, nssv674786, nssv660085, nssv676204, nssv687745, nssv685526, nssv690619, nssv690114, nssv693219, nssv675840
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516782
Frequency
Sample Size2026
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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