A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140857



Internal ID19258189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:149261244..149261313hg38UCSC Ensembl
Outerchr7:148958335..148958404hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992358
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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