A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561041



Internal ID18859322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27646266..27749600hg38UCSC Ensembl
Innerchr17:25973292..26076626hg19UCSC Ensembl
Innerchr17:22997419..23100753hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38103335
hg19103335
hg18103335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064417
Supporting Variants
Samples
Known GenesLGALS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561041
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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