A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517596



Internal ID15098203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98827414..98831573hg38UCSC Ensembl
Innerchr6:99275290..99279449hg19UCSC Ensembl
Innerchr6:99382011..99386170hg18UCSC Ensembl
Innerchr6:99382011..99386170hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg384160
hg194160
hg184160
hg174160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691298, nssv667969, nssv688364, nssv671362, nssv684513, nssv691211, nssv661947, nssv681049, nssv679250, nssv686391, nssv686474, nssv661887, nssv654130, nssv662128, nssv673131, nssv672036, nssv677904, nssv675681, nssv691661, nssv678381, nssv655954, nssv683368, nssv688826, nssv673229, nssv659180, nssv676967, nssv657432, nssv663176, nssv673116, nssv682993, nssv655222, nssv661480, nssv658756, nssv673934
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517596
Frequency
Sample Size2026
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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