A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024046



Internal ID18766579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:77643730..77678978hg38UCSC Ensembl
Innerchr7:77273047..77308295hg19UCSC Ensembl
Innerchr7:77110983..77146231hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3835249
hg1935249
hg1835249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6510n100
Supporting Variantsnssv3755403
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)nsv1024046
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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