A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607702



Internal ID16395111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83142079..83202742hg38UCSC Ensembl
Innerchr7:82771395..82832058hg19UCSC Ensembl
Innerchr7:82609331..82669994hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3860664
hg1960664
hg1860664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155223
SamplesNINDS_127
Known GenesPCLO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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