A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126191



Internal ID19259041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:32539599..32540099hg38UCSC Ensembl
Outerchr1:33005200..33005700hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv72n106
Supporting Variantsnssv3984420
SamplesKWS1
Known GenesZBTB8A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126191
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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