A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957176



Internal ID17306049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:155874498..155875234hg38UCSC Ensembl
Outerchr1:155844289..155845025hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004993
SamplesBILGI_BIOE
Known GenesSYT11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957176
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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