A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015660



Internal ID19104878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123954074..124076857hg38UCSC Ensembl
Innerchr6:124275219..124398002hg19UCSC Ensembl
Innerchr6:124316918..124439701hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38122784
hg19122784
hg18122784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654351
Samples
Known GenesNKAIN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015660
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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