A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3676736



Internal ID18628331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142706976..142795888hg38UCSC Ensembl
Innerchr7:142094383..142203700hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3888913
hg18109318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028035
Supporting Variants
Samples
Known GenesPRSS1, PRSS2, PRSS3P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3676736
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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