A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996032



Internal ID15234892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:64041483..64196113hg38UCSC Ensembl
Innerchr17:62118843..62273473hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38154631
hg19154631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483108
Supporting Variants
Samples
Known GenesERN1, SNORA76, SNORD104, TEX2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996032
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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