A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3477661



Internal ID18720982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16931632hg38UCSC Ensembl
Innerchr1:16871266..17258127hg19UCSC Ensembl
Innerchr1:16743853..17130714hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38386862
hg19386862
hg18386862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014932
Supporting Variants
Samples
Known GenesCROCC, CROCCP2, 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)nssv3477661
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