A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031904



Internal ID19121126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118495675..118545648hg38UCSC Ensembl
Innerchr7:118135729..118185702hg19UCSC Ensembl
Innerchr7:117922965..117972938hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3849974
hg1949974
hg1849974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662066
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)nsv1031904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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