A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704587



Internal ID15441239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88717509..88722643hg38UCSC Ensembl
Innerchr6:89427228..89432362hg19UCSC Ensembl
Innerchr6:89483947..89489081hg18UCSC Ensembl
Innerchr6:89483947..89489081hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385135
hg195135
hg185135
hg175135
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528054
Supporting Variants
Samples
Known GenesRNGTT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704587
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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