A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011863



Internal ID18754398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16864355..16921891hg38UCSC Ensembl
Innerchr1:17190850..17248386hg19UCSC Ensembl
Innerchr1:17063437..17120973hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3857537
hg1957537
hg1857537
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109n100
Supporting Variantsnssv3476822, nssv3700156, nssv3470824, nssv3481275, nssv3476424, nssv3464533, nssv3700158, nssv3465497, nssv3477309, nssv3700157, nssv3463593
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011863
Frequency
Sample Size29084
Observed Gain5
Observed Loss6
Observed Complex0
Frequencyn/a


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