A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055155



Internal ID18797686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57535839..57616251hg38UCSC Ensembl
Innerchr17:55613200..55693612hg19UCSC Ensembl
Innerchr17:52968199..53048611hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3880413
hg1980413
hg1880413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567703
Samples
Known GenesMSI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055155
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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