A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145176



Internal ID18902624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:226152881..226153085hg38UCSC Ensembl
Outerchr2:227017597..227017801hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2161n106
Supporting Variantsnssv3982260
SamplesKWS1
Known GenesLOC646736
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145176
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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