A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608315



Internal ID16395724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119294410..119521689hg38UCSC Ensembl
Innerchr7:118934464..119161743hg19UCSC Ensembl
Innerchr7:118721700..118948979hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38227280
hg19227280
hg18227280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11602n54
Supporting Variantsnssv1093575
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608315
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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