A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996238



Internal ID15235098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70031519..70218119hg38UCSC Ensembl
Innerchr17:68027660..68214260hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38186601
hg19186601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483015
Supporting Variants
Samples
Known GenesKCNJ16, KCNJ2, KCNJ2-AS1, LINC01028
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996238
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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