A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031824



Internal ID19121046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108295461..108365594hg38UCSC Ensembl
Innerchr7:107935905..108006038hg19UCSC Ensembl
Innerchr7:107723141..107793274hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3870134
hg1970134
hg1870134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6549n100
Supporting Variantsnssv3656222
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)nsv1031824
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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