A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027798



Internal ID19117016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156494660..156518254hg38UCSC Ensembl
Innerchr7:156287354..156310948hg19UCSC Ensembl
Innerchr7:155980115..156003709hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3823595
hg1923595
hg1823595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674701, nssv3674702, nssv3674703, nssv3674704
Samples
Known GenesLINC01006
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027798
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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