A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027661



Internal ID18770193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72640253..72900342hg38UCSC Ensembl
Innerchr7:72105238..72370879hg19UCSC Ensembl
Innerchr7:71743174..72008815hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38260090
hg19265642
hg18265642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6462n100
Supporting Variantsnssv3656470
Samples
Known GenesMIR4650-1, MIR4650-2, POM121, SBDSP1, SPDYE7P, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027661
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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