A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3751263



Internal ID18702858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:97294512..97755448hg38UCSC Ensembl
Innerchr6:97742388..98203324hg19UCSC Ensembl
Innerchr6:97849109..98310045hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38460937
hg19460937
hg18460937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017543
Supporting Variants
Samples
Known GenesMIR548H3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3751263
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