A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465207



Internal ID18714434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16691023..16932813hg38UCSC Ensembl
Innerchr1:17017518..17259308hg19UCSC Ensembl
Innerchr1:16890105..17131895hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38241791
hg19241791
hg18241791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999527
Supporting Variants
Samples
Known GenesCROCC, ESPNP, LOC729574, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3465207
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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