A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3698860



Internal ID18650455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16559628..16785052hg38UCSC Ensembl
Innerchr1:16886123..17111547hg19UCSC Ensembl
Innerchr1:16758710..16984134hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38225425
hg19225425
hg18225425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002636
Supporting Variants
Samples
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1L, 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)nssv3698860
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