A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126808



Internal ID18929571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:130668360..130668960hg38UCSC Ensembl
Outerchr7:130353200..130353800hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985083
SamplesKWS1
Known GenesCOPG2, TSGA13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126808
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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