A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987757



Internal ID18866560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:53990702..54001602hg38UCSC Ensembl
Outerchr6:53855500..53866400hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3810901
hg1910901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132963
Supporting Variants
SamplesKWS1
Known GenesMLIP-IT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987757
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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