A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757719



Internal ID19056000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146955070..146983237hg38UCSC Ensembl
Innerchr7:146652162..146680329hg19UCSC Ensembl
Innerchr7:146283095..146311262hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3828168
hg1928168
hg1828168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019300
Supporting Variants
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757719
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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