A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517287



Internal ID15097894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48914136..48926221hg38UCSC Ensembl
Innerchr10:50122181..50134266hg19UCSC Ensembl
Innerchr10:49792187..49804272hg18UCSC Ensembl
Innerchr10:49792187..49804272hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3812086
hg1912086
hg1812086
hg1712086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663231, nssv696227, nssv675486, nssv654204, nssv681137, nssv692163, nssv677120, nssv682901, nssv666146
Samples
Known GenesLRRC18, WDFY4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517287
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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