A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648957



Internal ID18947238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91271156..91407091hg38UCSC Ensembl
Innerchr6:91980874..92116809hg19UCSC Ensembl
Innerchr6:92037595..92173530hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38135936
hg19135936
hg18135936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030361
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)nssv3648957
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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