A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3676734



Internal ID18628329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142694837..142768033hg38UCSC Ensembl
Innerchr7:142402650..142476921hg19UCSC Ensembl
Innerchr7:142082232..142156496hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3873197
hg1974272
hg1874265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024031
Supporting Variants
Samples
Known GenesPRSS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3676734
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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