A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830637



Internal ID6156361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:33329365..33510704hg19UCSC Ensembl
Outerchr6:33437343..33618682hg18UCSC Ensembl
Outerchr6:33437343..33618682hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1445376, nssv1445377
Samples
Known GenesCUTA, KIFC1, PHF1, SYNGAP1, ZBTB9
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv830637
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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