A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981126



Internal ID19222560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7599214..7600814hg38UCSC Ensembl
Outerchr19:7664100..7665700hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118812
Supporting Variants
SamplesKWS1
Known GenesCAMSAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981126
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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