A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023222



Internal ID19112439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112794358..112836701hg38UCSC Ensembl
Innerchr7:112434413..112476756hg19UCSC Ensembl
Innerchr7:112221649..112263992hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3842344
hg1942344
hg1842344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6589n100
Supporting Variantsnssv3662035, nssv3662034, nssv3662032, nssv3662031, nssv3662033
Samples
Known GenesC7orf60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023222
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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