A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170264



Internal ID21314325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:51591243..51610762hg38UCSC Ensembl
Outerchr6:51584008..51611615hg38UCSC Ensembl
Innerchr6:51456041..51475560hg19UCSC Ensembl
Outerchr6:51448806..51476413hg19UCSC Ensembl
Innerchr6:51564000..51583519hg18UCSC Ensembl
Outerchr6:51556765..51584372hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3827608
hg1927608
hg1827608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251301
SamplesSNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170264
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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