A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136194



Internal ID18922007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40441101..40441701hg38UCSC Ensembl
Outerchr15:40733300..40733900hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967154, nssv3981323
SamplesKWS2, KWS1
Known GenesBAHD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136194
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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