A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094849



Internal ID15601349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140408296..140517870hg38UCSC Ensembl
Innerchr7:140108096..140217670hg19UCSC Ensembl
Innerchr7:139754565..139864139hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38109575
hg19109575
hg18109575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608500
Supporting Variants
Samples
Known GenesMKRN1, RAB19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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