A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022925



Internal ID19112142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91765445..91807800hg38UCSC Ensembl
Innerchr6:92475163..92517518hg19UCSC Ensembl
Innerchr6:92531884..92574239hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3842356
hg1942356
hg1842356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648966, nssv3648967
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)nsv1022925
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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