A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690114



Internal ID15080080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143133530..143175288hg38UCSC Ensembl
Innerchr7:142830623..142872381hg19UCSC Ensembl
Innerchr7:142540745..142582503hg18UCSC Ensembl
Innerchr7:142347460..142389218hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3841759
hg1941759
hg1841759
hg1741759
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516782
Supporting Variants
Samples
Known GenesPIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690114
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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