A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3742897



Internal ID18694492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99102848..99212536hg38UCSC Ensembl
Innerchr4:100023999..100133693hg19UCSC Ensembl
Innerchr4:100243022..100352716hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38109689
hg19109695
hg18109695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002574
Supporting Variants
Samples
Known GenesADH4, ADH6, LOC100507053, PCNAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3742897
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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