A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691265



Internal ID18989546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105911241..105946847hg38UCSC Ensembl
Innerchr8:106923469..106959075hg19UCSC Ensembl
Innerchr8:106992645..107028251hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3835607
hg1935607
hg1835607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019518
Supporting Variants
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)nssv3691265
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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