A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155882



Internal ID15531776
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 StatusS
Merged Variantsnsv608608
Supporting Variants
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)nssv1155882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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