A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515723



Internal ID15096330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98388419..98435072hg38UCSC Ensembl
Innerchr10:100148176..100194829hg19UCSC Ensembl
Innerchr10:100138166..100184819hg18UCSC Ensembl
Innerchr10:100138166..100184819hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3846654
hg1946654
hg1846654
hg1746654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705981, nssv664560, nssv679417, nssv683458, nssv697367, nssv701731, nssv668327
Samples
Known GenesHPS1, MIR1287, MIR4685, PYROXD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515723
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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