A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029719



Internal ID18772250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142535861..142763407hg38UCSC Ensembl
Innerchr7:141924465..142150831hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38227547
hg18226367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752190
Samples
Known GenesMTRNR2L6, PRSS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029719
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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