A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965487



Internal ID18898142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:14486769..14492729hg38UCSC Ensembl
Outerchr12:14639703..14645663hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg385961
hg195961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121486
Supporting Variants
SamplesKWS2
Known GenesATF7IP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965487
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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