A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567824



Internal ID18519419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78601694..78666124hg38UCSC Ensembl
Innerchr17:76597776..76662206hg19UCSC Ensembl
Innerchr17:74109371..74173801hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3864431
hg1964431
hg1864431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066466
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)nssv3567824
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer