A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758855



Internal ID17510728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57039159..57090985hg38UCSC Ensembl
Innerchr6:56903957..56955783hg19UCSC Ensembl
Innerchr6:57011916..57063742hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3851827
hg1951827
hg1851827
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv970717
Supporting Variants
SamplesHGDP01029
Known GenesKIAA1586, ZNF451
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758855
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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