A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605584



Internal ID16392993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20403..68920hg38UCSC Ensembl
Innerchr7:20403..68920hg19UCSC Ensembl
Innerchr7:113336..164003hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3848518
hg1948518
hg1850668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077596, nssv1077590, nssv1077594, nssv1077591, nssv1077595, nssv1077589, nssv1077592, nssv1077593
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605584
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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