A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958544



Internal ID19203835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:108440279..108440343hg38UCSC Ensembl
Outerchr6:108761483..108761547hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128269
Supporting Variants
SamplesKWS1
Known GenesLACE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958544
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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