A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469714



Internal ID15534429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45277907..45434085hg38UCSC Ensembl
Innerchr7:45317506..45473684hg19UCSC Ensembl
Innerchr7:45284031..45440209hg18UCSC Ensembl
Innerchr7:45058286..45214464hg16UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38156179
hg19156179
hg18156179
hg16156179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676649, nssv1673325, nssv1674622, nssv1672693, nssv1674252, nssv1673472, nssv1672658, nssv1674799, nssv1673134, nssv1674452, nssv1672878, nssv1672447, nssv1674063, nssv1676363, nssv1674013, nssv1673129, nssv1672410, nssv1675159, nssv1673594, nssv1675893, nssv1675061, nssv1676203, nssv1674446, nssv1674887, nssv1674920, nssv1673775, nssv1673438, nssv1673924, nssv1675172, nssv1673587, nssv1672961
Samples
Known Genes
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469714
Frequency
Sample Size265
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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