A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029103



Internal ID19118322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118277308..118395933hg38UCSC Ensembl
Innerchr7:117917362..118035987hg19UCSC Ensembl
Innerchr7:117704598..117823223hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38118626
hg19118626
hg18118626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662063, nssv3662060, nssv3662058, nssv3662062, nssv3662059, nssv3662061, nssv3751517, nssv3751516
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)nsv1029103
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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