A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3463666



Internal ID18713599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16583102..16685949hg38UCSC Ensembl
Innerchr1:16909597..17012444hg19UCSC Ensembl
Innerchr1:16782184..16885031hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38102848
hg19102848
hg18102848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997399
Supporting Variants
Samples
Known GenesCROCCP2, LOC729574, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3463666
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