A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985944



Internal ID18876733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:51871334..51872006hg38UCSC Ensembl
Outerchr6:51736132..51736804hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131523
Supporting Variants
SamplesKWS1
Known GenesPKHD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985944
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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