A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006754



Internal ID18749285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25256126..25320483hg38UCSC Ensembl
Innerchr1:25582617..25646974hg19UCSC Ensembl
Innerchr1:25455204..25519561hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3864358
hg1964358
hg1864358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv134n100
Supporting Variantsnssv3473665, nssv3464590, nssv3480601, nssv3478471, nssv3466316, nssv3465036, nssv3481570, nssv3472569, nssv3477583, nssv3475736, nssv3475037, nssv3700866, nssv3700865
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006754
Frequency
Sample Size29084
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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