A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608608



Internal ID16049331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142423435..142785320hg38UCSC Ensembl
Innerchr7:141791880..142193132hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38361886
hg18401253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11644n54
Supporting Variantsnssv1155882
SamplesHGDP01205
Known GenesMTRNR2L6, PRSS1, PRSS2, PRSS3P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608608
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer