A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3467968



Internal ID18715911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16544771..16691123hg38UCSC Ensembl
Innerchr1:16871266..17017618hg19UCSC Ensembl
Innerchr1:16743853..16890205hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38146353
hg19146353
hg18146353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004053
Supporting Variants
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)nssv3467968
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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