A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015646



Internal ID18758180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6698852..6739639hg38UCSC Ensembl
Innerchr7:6738483..6779270hg19UCSC Ensembl
Innerchr7:6705008..6745795hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3840788
hg1940788
hg1840788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752810, nssv3752811
Samples
Known GenesPMS2CL, ZNF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015646
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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