A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145142



Internal ID18937731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:73596870..73597670hg38UCSC Ensembl
Outerchr7:73011200..73012000hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982224
SamplesKWS1
Known GenesMLXIPL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145142
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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