A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027369



Internal ID19116588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127132057..127158817hg38UCSC Ensembl
Innerchr7:126772111..126798871hg19UCSC Ensembl
Innerchr7:126559347..126586107hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3826761
hg1926761
hg1826761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662178
Samples
Known GenesGRM8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027369
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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