A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982244



Internal ID18863282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:140009500..140010100hg38UCSC Ensembl
Outerchr7:139709300..139709900hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145162
Supporting Variants
SamplesKWS1
Known GenesTBXAS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982244
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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