A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3482260



Internal ID18723452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16898718hg38UCSC Ensembl
Innerchr1:16871266..17225213hg19UCSC Ensembl
Innerchr1:16743853..17097800hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38353948
hg19353948
hg18353948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008791
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)nssv3482260
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