A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014522



Internal ID18757056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16934586hg38UCSC Ensembl
Innerchr1:16871266..17261081hg19UCSC Ensembl
Innerchr1:16743853..17133668hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38389816
hg19389816
hg18389816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39n100
Supporting Variantsnssv3477728
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)nsv1014522
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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