A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996249



Internal ID15581750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154833739..154996113hg38UCSC Ensembl
Innerchr7:154625449..154787823hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38162375
hg19162375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483088
Supporting Variants
Samples
Known GenesDPP6, PAXIP1, PAXIP1-AS2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996249
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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