A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006615



Internal ID18749146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16689670hg38UCSC Ensembl
Innerchr1:16871266..17016165hg19UCSC Ensembl
Innerchr1:16743853..16888752hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38144900
hg19144900
hg18144900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n100
Supporting Variantsnssv3474643, nssv3476449
Samples
Known GenesCROCCP2, LOC729574, MIR3675, 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)nsv1006615
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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