A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996205



Internal ID15235065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78607335..78727244hg38UCSC Ensembl
Innerchr17:76603417..76723326hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38119910
hg19119910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv482920
Supporting Variants
Samples
Known GenesCYTH1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996205
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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