A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155784



Internal ID15853365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:136476073..136676481hg38UCSC Ensembl
Innerchr6:136797211..136997619hg19UCSC Ensembl
Innerchr6:136838904..137039312hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38200409
hg19200409
hg18200409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604725
Supporting Variants
Samples1780854123_A
Known GenesMAP3K5, MAP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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