A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015501



Internal ID19104718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:100630013..100654559hg38UCSC Ensembl
Innerchr8:101642241..101666787hg19UCSC Ensembl
Innerchr8:101711417..101735963hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3824547
hg1924547
hg1824547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757330
Samples
Known GenesSNX31
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015501
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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