A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021783



Internal ID19111001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108295461..108357837hg38UCSC Ensembl
Innerchr7:107935905..107998281hg19UCSC Ensembl
Innerchr7:107723141..107785517hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3862377
hg1962377
hg1862377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6549n100
Supporting Variantsnssv3656221, nssv3755481
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)nsv1021783
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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