A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011075



Internal ID18753609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61469634..61503171hg38UCSC Ensembl
Innerchr1:61935306..61968843hg19UCSC Ensembl
Innerchr1:61707894..61741431hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3833538
hg1933538
hg1833538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3474601, nssv3476530, nssv3465013
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)nsv1011075
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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