A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015383



Internal ID19104600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109675755..109945605hg38UCSC Ensembl
Innerchr7:109315812..109585662hg19UCSC Ensembl
Innerchr7:109103048..109372898hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38269851
hg19269851
hg18269851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656234
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)nsv1015383
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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