A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724977



Internal ID19023258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52192992..52243307hg38UCSC Ensembl
Innerchr17:50270352..50320667hg19UCSC Ensembl
Innerchr17:47625351..47675666hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3850316
hg1950316
hg1850316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064193
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)nssv3724977
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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