A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023262



Internal ID18765794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88708079..90287629hg38UCSC Ensembl
Innerchr7:88337393..89916943hg19UCSC Ensembl
Innerchr7:88175329..89754879hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381579551
hg191579551
hg181579551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6525n100
Supporting Variantsnssv3655206
Samples
Known GenesC7orf62, C7orf63, DPY19L2P4, STEAP1, STEAP2, ZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023262
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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