A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007096



Internal ID18749627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16679269hg38UCSC Ensembl
Innerchr1:16871266..17005764hg19UCSC Ensembl
Innerchr1:16743853..16878351hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38134499
hg19134499
hg18134499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n100
Supporting Variantsnssv3698831, nssv3698829, nssv3698830, nssv3698832, nssv3472046
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)nsv1007096
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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