A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136273



Internal ID19274318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7599314..7600914hg38UCSC Ensembl
Outerchr19:7664200..7665800hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1703n106
Supporting Variantsnssv3989889
SamplesKWS2
Known GenesCAMSAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136273
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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