A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016264



Internal ID19105483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118099092..118152934hg38UCSC Ensembl
Innerchr7:117739146..117792988hg19UCSC Ensembl
Innerchr7:117526382..117580224hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3853843
hg1953843
hg1853843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6595n100
Supporting Variantsnssv3662055, nssv3662056, nssv3751515
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016264
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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