A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908900



Internal ID6270827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76918131..77003357hg19UCSC Ensembl
Outerchr17:76907353..77033092hg19UCSC Ensembl
Innerchr17:74429726..74514952hg18UCSC Ensembl
Outerchr17:74418948..74544687hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1599448, nssv1538722
SamplesIS41634, MS13770
Known GenesC1QTNF1, CANT1, LGALS3BP, LOC100507410, TIMP2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908900
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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