A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607736



Internal ID16395145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88039690..88043111hg38UCSC Ensembl
Innerchr7:87669005..87672426hg19UCSC Ensembl
Innerchr7:87506941..87510362hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg383422
hg193422
hg183422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11491n54
Supporting Variantsnssv1089412, nssv1089411, nssv1089406, nssv1089414, nssv1089426, nssv1089407, nssv1089410, nssv1089404, nssv1089413, nssv1089425, nssv1089408, nssv1089428, nssv1089421, nssv1089422, nssv1089420, nssv1089424, nssv1089418, nssv1089416, nssv1089409, nssv1089423, nssv1089405, nssv1089417, nssv1089427, nssv1089415, nssv1089419
Samples
Known GenesADAM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607736
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer