A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466004



Internal ID18714841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16902199hg38UCSC Ensembl
Innerchr1:16871266..17228694hg19UCSC Ensembl
Innerchr1:16743853..17101281hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38357429
hg19357429
hg18357429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998219
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)nssv3466004
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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