A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006849



Internal ID18749380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16627264..16643949hg38UCSC Ensembl
Innerchr1:16953759..16970444hg19UCSC Ensembl
Innerchr1:16826346..16843031hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816686
hg1916686
hg1816686
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3475522, nssv3463231, nssv3471099, nssv3477604
Samples
Known GenesCROCCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006849
Frequency
Sample Size29084
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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