A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126742



Internal ID18939078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:2764966..2766366hg38UCSC Ensembl
Outerchr6:2765200..2766600hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985010
SamplesKWS1
Known GenesWRNIP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126742
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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