A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984590



Internal ID19204578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:97976246..97976846hg38UCSC Ensembl
Outerchr13:98628500..98629100hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126350
Supporting Variants
SamplesKWS1
Known GenesIPO5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984590
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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