A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035092



Internal ID19124311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76802993..77093126hg38UCSC Ensembl
Innerchr7:76432310..76722443hg19UCSC Ensembl
Innerchr7:76270246..76560379hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38290134
hg19290134
hg18290134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6501n100
Supporting Variantsnssv3657028
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035092
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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