A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030698



Internal ID18773229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132094168..132130552hg38UCSC Ensembl
Innerchr7:131778927..131815311hg19UCSC Ensembl
Innerchr7:131429467..131465851hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3836385
hg1936385
hg1836385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662206
Samples
Known GenesPLXNA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030698
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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