A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975126



Internal ID19235705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:73780742..73780832hg38UCSC Ensembl
Outerchr6:74490465..74490555hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114840
Supporting Variants
SamplesKWS2
Known GenesCD109
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975126
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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