A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018379



Internal ID18760912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38277957..38309326hg38UCSC Ensembl
Innerchr7:38317558..38348927hg19UCSC Ensembl
Innerchr7:38284083..38315452hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3831370
hg1931370
hg1831370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6329n100
Supporting Variantsnssv3643465
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)nsv1018379
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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