A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014380



Internal ID18756914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16864355..16931632hg38UCSC Ensembl
Innerchr1:17190850..17258127hg19UCSC Ensembl
Innerchr1:17063437..17130714hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3867278
hg1967278
hg1867278
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n100
Supporting Variantsnssv3467907, nssv3700160, nssv3474542, nssv3462958, nssv3472910, nssv3463806, nssv3470175, nssv3463975, nssv3472001, nssv3466793, nssv3476150, nssv3700159
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014380
Frequency
Sample Size29084
Observed Gain4
Observed Loss8
Observed Complex0
Frequencyn/a


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