A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567702



Internal ID18865983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57321283..57373857hg38UCSC Ensembl
Innerchr17:55398644..55451218hg19UCSC Ensembl
Innerchr17:52753643..52806217hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3852575
hg1952575
hg1852575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064897
Supporting Variants
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)nssv3567702
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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