A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908903



Internal ID6270830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76964309..77003357hg19UCSC Ensembl
Outerchr17:76962059..77033092hg19UCSC Ensembl
Innerchr17:74475904..74514952hg18UCSC Ensembl
Outerchr17:74473654..74544687hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1573945
SamplesIS33504
Known GenesC1QTNF1, CANT1, LGALS3BP, LOC100507410
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908903
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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