A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654786



Internal ID18606381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10486213..10558057hg38UCSC Ensembl
Innerchr6:10486446..10558290hg19UCSC Ensembl
Innerchr6:10594432..10666276hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3871845
hg1971845
hg1871845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023083
Supporting Variants
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3654786
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