A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560547



Internal ID18858828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19591542..19634157hg38UCSC Ensembl
Innerchr17:19494855..19537470hg19UCSC Ensembl
Innerchr17:19435447..19478062hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3842616
hg1942616
hg1842616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056466
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560547
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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