A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606628



Internal ID16047351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38248669..38301625hg38UCSC Ensembl
Innerchr7:38288270..38341226hg19UCSC Ensembl
Innerchr7:38254795..38307751hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3852957
hg1952957
hg1852957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11275n54
Supporting Variantsnssv1082713, nssv1082712, nssv1082711, nssv1082714
Samples
Known GenesTARP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606628
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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