A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002758



Internal ID18745290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16850538..16959812hg38UCSC Ensembl
Innerchr1:17177033..17286307hg19UCSC Ensembl
Innerchr1:17049620..17158894hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38109275
hg19109275
hg18109275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv107n100
Supporting Variantsnssv3477289, nssv3475308, nssv3479361, nssv3475273, nssv3469330, nssv3465102, nssv3468123, nssv3478269
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002758
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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