A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983551



Internal ID19236343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7201822..7232666hg38UCSC Ensembl
Outerchr19:7201833..7232677hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3830845
hg1930845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125376
Supporting Variants
SamplesKWS2
Known GenesINSR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983551
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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