A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019059



Internal ID19108276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108295461..108355079hg38UCSC Ensembl
Innerchr7:107935905..107995523hg19UCSC Ensembl
Innerchr7:107723141..107782759hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3859619
hg1959619
hg1859619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6549n100
Supporting Variantsnssv3656220
Samples
Known GenesNRCAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019059
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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