A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607732



Internal ID16048455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88039690..88041845hg38UCSC Ensembl
Innerchr7:87669005..87671160hg19UCSC Ensembl
Innerchr7:87506941..87509096hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382156
hg192156
hg182156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11490n54
Supporting Variantsnssv1089393, nssv1089397, nssv1089398, nssv1089396, nssv1089394, nssv1089395
Samples
Known GenesADAM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607732
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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