A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017288



Internal ID19106505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108299295..108360393hg38UCSC Ensembl
Innerchr7:107939739..108000837hg19UCSC Ensembl
Innerchr7:107726975..107788073hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3861099
hg1961099
hg1861099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6549n100
Supporting Variantsnssv3656223
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)nsv1017288
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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