A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655758



Internal ID18607353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27512448..27637542hg38UCSC Ensembl
Innerchr6:27480227..27605321hg19UCSC Ensembl
Innerchr6:27588206..27713300hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38125095
hg19125095
hg18125095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025862
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655758
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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